Multicomponent Synthesis : : Bioactive Heterocycles / / ed. by Basudeb Basu, Bubun Banerjee.
Multicomponent synthesis may provide new and green routes for obtaining bioactive heterocycles. These methods produce less organic waste due to no longer removing solvent and other components between reaction steps. It can be applied to the synthesis of heterocycles with reactions such as the Bigine...
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Place / Publishing House: | Berlin ;, Boston : : De Gruyter, , [2023] ©2024 |
Year of Publication: | 2023 |
Language: | English |
Series: | Green Bioactive Heterocycles ,
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Multicomponent Synthesis : Bioactive Heterocycles / ed. by Basudeb Basu, Bubun Banerjee. Berlin ; Boston : De Gruyter, [2023] ©2024 1 online resource (XV, 433 p.) text txt rdacontent computer c rdamedia online resource cr rdacarrier text file PDF rda Green Bioactive Heterocycles , 2752-1338 ; 5 Frontmatter -- Preface -- Foreword -- A brief professional profile of Prof. Eric F.V. Scriven -- Contents -- List of contributing authors -- 1 Synthesis of aza-heterocycles via one-pot domino multicomponent reaction approach -- 2 One-pot three-component selective annulation strategies for the synthesis of bioactive β-lactam, pyrrole, and pyridine scaffolds -- 3 One-pot three-component synthesis of quinolines and some other selective six-membered heterocycles with biological importance -- 4 Multicomponent synthesis of biologically prominent tetrahydrobenzoxanthenone derivatives -- 5 One-pot five/four-component synthesis of structurally diverse bioactive quinoxaline-annulated spiroheterocycles through the in situ formation of 11Hindeno[ 1,2-b]quinoxalin-11-ones -- 6 Multicomponent synthesis of biologically active quinazolinone derivatives -- 7 Recent approaches toward the synthesis of 1,2,3-triazoles using multicomponent techniques -- 8 Synthesis of various bioactive tetrazoles via one-pot multicomponent click reactions -- 9 L-Proline and its derivatives catalyzed one-pot multicomponent synthesis of biologically promising N- and O-heterocycles -- 10 Microwave-assisted solvent-free multicomponent synthesis of bioactive heterocycles -- 11 Deep eutectic mixture (DEM)-assisted multicomponent synthesis of heterocycles -- Index restricted access http://purl.org/coar/access_right/c_16ec online access with authorization star Multicomponent synthesis may provide new and green routes for obtaining bioactive heterocycles. These methods produce less organic waste due to no longer removing solvent and other components between reaction steps. It can be applied to the synthesis of heterocycles with reactions such as the Biginelli reaction. This book explores the use of multi-component reactions for various heterocyclic structures with bioactivity. Issued also in print. Mode of access: Internet via World Wide Web. In English. Description based on online resource; title from PDF title page (publisher's Web site, viewed 06. Mrz 2024) Organische Chemie. Synthese. grüne Chemie. SCIENCE / Chemistry / General. bisacsh Atom efficiency. Biginelli Reaction. Domino Reactions. Green Chemistry. Green Synthesis. Ionic Liquids. Magnetic Nanocatalysis. Multicomponent Reactions. One-pot Synthesis. Sustainable Developments. Amaregouda, Yamanappagouda, contributor. ctb https://id.loc.gov/vocabulary/relators/ctb Banerjee, Bubun, contributor. ctb https://id.loc.gov/vocabulary/relators/ctb Banerjee, Bubun, editor. edt http://id.loc.gov/vocabulary/relators/edt Basu, Basudeb, contributor. ctb https://id.loc.gov/vocabulary/relators/ctb Basu, Basudeb, editor. edt http://id.loc.gov/vocabulary/relators/edt Biswas, Soumili, contributor. ctb https://id.loc.gov/vocabulary/relators/ctb Chakraborti, Asit K., contributor. ctb https://id.loc.gov/vocabulary/relators/ctb Das, Asish R., contributor. ctb https://id.loc.gov/vocabulary/relators/ctb Dhara, Samiran, contributor. ctb https://id.loc.gov/vocabulary/relators/ctb Durga Nageswar, Yadavalli Venkata, contributor. ctb https://id.loc.gov/vocabulary/relators/ctb Ghosh, Sujit, contributor. ctb https://id.loc.gov/vocabulary/relators/ctb Islam, Saiful, contributor. ctb https://id.loc.gov/vocabulary/relators/ctb Kamanna, Kantharaju, contributor. ctb https://id.loc.gov/vocabulary/relators/ctb Kamath, Aravind, contributor. ctb https://id.loc.gov/vocabulary/relators/ctb Kaur, Manmeet, contributor. ctb https://id.loc.gov/vocabulary/relators/ctb Mane, Radhika, contributor. ctb https://id.loc.gov/vocabulary/relators/ctb Mathew, Bijoy P., contributor. ctb https://id.loc.gov/vocabulary/relators/ctb Nath, Mahendra, contributor. ctb https://id.loc.gov/vocabulary/relators/ctb Patel, Divyang M., contributor. ctb https://id.loc.gov/vocabulary/relators/ctb Patel, Hitendra M., contributor. ctb https://id.loc.gov/vocabulary/relators/ctb Priya, Anu, contributor. ctb https://id.loc.gov/vocabulary/relators/ctb Rakhi, Katla, contributor. ctb https://id.loc.gov/vocabulary/relators/ctb Ramesh, Katla, contributor. ctb https://id.loc.gov/vocabulary/relators/ctb Rao, Vaidya Jayathirtha, contributor. ctb https://id.loc.gov/vocabulary/relators/ctb Saha, Nirjhar, contributor. ctb https://id.loc.gov/vocabulary/relators/ctb Sai Pavan Kumar, Ch. N. S., contributor. ctb https://id.loc.gov/vocabulary/relators/ctb Sarkar, Anirban, contributor. ctb https://id.loc.gov/vocabulary/relators/ctb Scriven, Eric F. V., contributor. ctb https://id.loc.gov/vocabulary/relators/ctb Sharma, Aditi, contributor. ctb https://id.loc.gov/vocabulary/relators/ctb Singh, Arvind, contributor. ctb https://id.loc.gov/vocabulary/relators/ctb Singh, Jagmeet, contributor. ctb https://id.loc.gov/vocabulary/relators/ctb Vaja, Maulikkumar D., contributor. ctb https://id.loc.gov/vocabulary/relators/ctb Title is part of eBook package: De Gruyter DG Plus DeG Package 2024 Part 1 9783111332192 Title is part of eBook package: De Gruyter EBOOK PACKAGE COMPLETE 2023 English 9783111319292 Title is part of eBook package: De Gruyter EBOOK PACKAGE COMPLETE 2023 9783111318912 ZDB-23-DGG Title is part of eBook package: De Gruyter EBOOK PACKAGE Physics, Chemistry, Mat.Sc, Geosc 2023 English 9783111319230 Title is part of eBook package: De Gruyter EBOOK PACKAGE Physics, Chemistry, Mat.Sc, Geosc 2023 9783111318660 ZDB-23-DPC EPUB 9783110986112 print 9783110997330 https://doi.org/10.1515/9783110985313 https://www.degruyter.com/isbn/9783110985313 Cover https://www.degruyter.com/document/cover/isbn/9783110985313/original |
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English |
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eBook |
author2 |
Amaregouda, Yamanappagouda, Amaregouda, Yamanappagouda, Banerjee, Bubun, Banerjee, Bubun, Banerjee, Bubun, Banerjee, Bubun, Basu, Basudeb, Basu, Basudeb, Basu, Basudeb, Basu, Basudeb, Biswas, Soumili, Biswas, Soumili, Chakraborti, Asit K., Chakraborti, Asit K., Das, Asish R., Das, Asish R., Dhara, Samiran, Dhara, Samiran, Durga Nageswar, Yadavalli Venkata, Durga Nageswar, Yadavalli Venkata, Ghosh, Sujit, Ghosh, Sujit, Islam, Saiful, Islam, Saiful, Kamanna, Kantharaju, Kamanna, Kantharaju, Kamath, Aravind, Kamath, Aravind, Kaur, Manmeet, Kaur, Manmeet, Mane, Radhika, Mane, Radhika, Mathew, Bijoy P., Mathew, Bijoy P., Nath, Mahendra, Nath, Mahendra, Patel, Divyang M., Patel, Divyang M., Patel, Hitendra M., Patel, Hitendra M., Priya, Anu, Priya, Anu, Rakhi, Katla, Rakhi, Katla, Ramesh, Katla, Ramesh, Katla, Rao, Vaidya Jayathirtha, Rao, Vaidya Jayathirtha, Saha, Nirjhar, Saha, Nirjhar, Sai Pavan Kumar, Ch. N. S., Sai Pavan Kumar, Ch. N. S., Sarkar, Anirban, Sarkar, Anirban, Scriven, Eric F. V., Scriven, Eric F. V., Sharma, Aditi, Sharma, Aditi, Singh, Arvind, Singh, Arvind, Singh, Jagmeet, Singh, Jagmeet, Vaja, Maulikkumar D., Vaja, Maulikkumar D., |
author_facet |
Amaregouda, Yamanappagouda, Amaregouda, Yamanappagouda, Banerjee, Bubun, Banerjee, Bubun, Banerjee, Bubun, Banerjee, Bubun, Basu, Basudeb, Basu, Basudeb, Basu, Basudeb, Basu, Basudeb, Biswas, Soumili, Biswas, Soumili, Chakraborti, Asit K., Chakraborti, Asit K., Das, Asish R., Das, Asish R., Dhara, Samiran, Dhara, Samiran, Durga Nageswar, Yadavalli Venkata, Durga Nageswar, Yadavalli Venkata, Ghosh, Sujit, Ghosh, Sujit, Islam, Saiful, Islam, Saiful, Kamanna, Kantharaju, Kamanna, Kantharaju, Kamath, Aravind, Kamath, Aravind, Kaur, Manmeet, Kaur, Manmeet, Mane, Radhika, Mane, Radhika, Mathew, Bijoy P., Mathew, Bijoy P., Nath, Mahendra, Nath, Mahendra, Patel, Divyang M., Patel, Divyang M., Patel, Hitendra M., Patel, Hitendra M., Priya, Anu, Priya, Anu, Rakhi, Katla, Rakhi, Katla, Ramesh, Katla, Ramesh, Katla, Rao, Vaidya Jayathirtha, Rao, Vaidya Jayathirtha, Saha, Nirjhar, Saha, Nirjhar, Sai Pavan Kumar, Ch. N. S., Sai Pavan Kumar, Ch. N. S., Sarkar, Anirban, Sarkar, Anirban, Scriven, Eric F. V., Scriven, Eric F. V., Sharma, Aditi, Sharma, Aditi, Singh, Arvind, Singh, Arvind, Singh, Jagmeet, Singh, Jagmeet, Vaja, Maulikkumar D., Vaja, Maulikkumar D., |
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author_sort |
Amaregouda, Yamanappagouda, |
title |
Multicomponent Synthesis : Bioactive Heterocycles / |
spellingShingle |
Multicomponent Synthesis : Bioactive Heterocycles / Green Bioactive Heterocycles , Frontmatter -- Preface -- Foreword -- A brief professional profile of Prof. Eric F.V. Scriven -- Contents -- List of contributing authors -- 1 Synthesis of aza-heterocycles via one-pot domino multicomponent reaction approach -- 2 One-pot three-component selective annulation strategies for the synthesis of bioactive β-lactam, pyrrole, and pyridine scaffolds -- 3 One-pot three-component synthesis of quinolines and some other selective six-membered heterocycles with biological importance -- 4 Multicomponent synthesis of biologically prominent tetrahydrobenzoxanthenone derivatives -- 5 One-pot five/four-component synthesis of structurally diverse bioactive quinoxaline-annulated spiroheterocycles through the in situ formation of 11Hindeno[ 1,2-b]quinoxalin-11-ones -- 6 Multicomponent synthesis of biologically active quinazolinone derivatives -- 7 Recent approaches toward the synthesis of 1,2,3-triazoles using multicomponent techniques -- 8 Synthesis of various bioactive tetrazoles via one-pot multicomponent click reactions -- 9 L-Proline and its derivatives catalyzed one-pot multicomponent synthesis of biologically promising N- and O-heterocycles -- 10 Microwave-assisted solvent-free multicomponent synthesis of bioactive heterocycles -- 11 Deep eutectic mixture (DEM)-assisted multicomponent synthesis of heterocycles -- Index |
title_sub |
Bioactive Heterocycles / |
title_full |
Multicomponent Synthesis : Bioactive Heterocycles / ed. by Basudeb Basu, Bubun Banerjee. |
title_fullStr |
Multicomponent Synthesis : Bioactive Heterocycles / ed. by Basudeb Basu, Bubun Banerjee. |
title_full_unstemmed |
Multicomponent Synthesis : Bioactive Heterocycles / ed. by Basudeb Basu, Bubun Banerjee. |
title_auth |
Multicomponent Synthesis : Bioactive Heterocycles / |
title_alt |
Frontmatter -- Preface -- Foreword -- A brief professional profile of Prof. Eric F.V. Scriven -- Contents -- List of contributing authors -- 1 Synthesis of aza-heterocycles via one-pot domino multicomponent reaction approach -- 2 One-pot three-component selective annulation strategies for the synthesis of bioactive β-lactam, pyrrole, and pyridine scaffolds -- 3 One-pot three-component synthesis of quinolines and some other selective six-membered heterocycles with biological importance -- 4 Multicomponent synthesis of biologically prominent tetrahydrobenzoxanthenone derivatives -- 5 One-pot five/four-component synthesis of structurally diverse bioactive quinoxaline-annulated spiroheterocycles through the in situ formation of 11Hindeno[ 1,2-b]quinoxalin-11-ones -- 6 Multicomponent synthesis of biologically active quinazolinone derivatives -- 7 Recent approaches toward the synthesis of 1,2,3-triazoles using multicomponent techniques -- 8 Synthesis of various bioactive tetrazoles via one-pot multicomponent click reactions -- 9 L-Proline and its derivatives catalyzed one-pot multicomponent synthesis of biologically promising N- and O-heterocycles -- 10 Microwave-assisted solvent-free multicomponent synthesis of bioactive heterocycles -- 11 Deep eutectic mixture (DEM)-assisted multicomponent synthesis of heterocycles -- Index |
title_new |
Multicomponent Synthesis : |
title_sort |
multicomponent synthesis : bioactive heterocycles / |
series |
Green Bioactive Heterocycles , |
series2 |
Green Bioactive Heterocycles , |
publisher |
De Gruyter, |
publishDate |
2023 |
physical |
1 online resource (XV, 433 p.) Issued also in print. |
contents |
Frontmatter -- Preface -- Foreword -- A brief professional profile of Prof. Eric F.V. Scriven -- Contents -- List of contributing authors -- 1 Synthesis of aza-heterocycles via one-pot domino multicomponent reaction approach -- 2 One-pot three-component selective annulation strategies for the synthesis of bioactive β-lactam, pyrrole, and pyridine scaffolds -- 3 One-pot three-component synthesis of quinolines and some other selective six-membered heterocycles with biological importance -- 4 Multicomponent synthesis of biologically prominent tetrahydrobenzoxanthenone derivatives -- 5 One-pot five/four-component synthesis of structurally diverse bioactive quinoxaline-annulated spiroheterocycles through the in situ formation of 11Hindeno[ 1,2-b]quinoxalin-11-ones -- 6 Multicomponent synthesis of biologically active quinazolinone derivatives -- 7 Recent approaches toward the synthesis of 1,2,3-triazoles using multicomponent techniques -- 8 Synthesis of various bioactive tetrazoles via one-pot multicomponent click reactions -- 9 L-Proline and its derivatives catalyzed one-pot multicomponent synthesis of biologically promising N- and O-heterocycles -- 10 Microwave-assisted solvent-free multicomponent synthesis of bioactive heterocycles -- 11 Deep eutectic mixture (DEM)-assisted multicomponent synthesis of heterocycles -- Index |
isbn |
9783110985313 9783111332192 9783111319292 9783111318912 9783111319230 9783111318660 9783110986112 9783110997330 |
issn |
2752-1338 ; |
url |
https://doi.org/10.1515/9783110985313 https://www.degruyter.com/isbn/9783110985313 https://www.degruyter.com/document/cover/isbn/9783110985313/original |
illustrated |
Not Illustrated |
dewey-hundreds |
500 - Science |
dewey-tens |
540 - Chemistry |
dewey-ones |
547 - Organic chemistry |
dewey-full |
547.2 |
dewey-sort |
3547.2 |
dewey-raw |
547.2 |
dewey-search |
547.2 |
doi_str_mv |
10.1515/9783110985313 |
oclc_num |
1415896501 |
work_keys_str_mv |
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is_hierarchy_title |
Multicomponent Synthesis : Bioactive Heterocycles / |
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Title is part of eBook package: De Gruyter DG Plus DeG Package 2024 Part 1 |
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Scriven -- </subfield><subfield code="t">Contents -- </subfield><subfield code="t">List of contributing authors -- </subfield><subfield code="t">1 Synthesis of aza-heterocycles via one-pot domino multicomponent reaction approach -- </subfield><subfield code="t">2 One-pot three-component selective annulation strategies for the synthesis of bioactive β-lactam, pyrrole, and pyridine scaffolds -- </subfield><subfield code="t">3 One-pot three-component synthesis of quinolines and some other selective six-membered heterocycles with biological importance -- </subfield><subfield code="t">4 Multicomponent synthesis of biologically prominent tetrahydrobenzoxanthenone derivatives -- </subfield><subfield code="t">5 One-pot five/four-component synthesis of structurally diverse bioactive quinoxaline-annulated spiroheterocycles through the in situ formation of 11Hindeno[ 1,2-b]quinoxalin-11-ones -- </subfield><subfield code="t">6 Multicomponent synthesis of biologically active quinazolinone derivatives -- </subfield><subfield code="t">7 Recent approaches toward the synthesis of 1,2,3-triazoles using multicomponent techniques -- </subfield><subfield code="t">8 Synthesis of various bioactive tetrazoles via one-pot multicomponent click reactions -- </subfield><subfield code="t">9 L-Proline and its derivatives catalyzed one-pot multicomponent synthesis of biologically promising N- and O-heterocycles -- </subfield><subfield code="t">10 Microwave-assisted solvent-free multicomponent synthesis of bioactive heterocycles -- </subfield><subfield code="t">11 Deep eutectic mixture (DEM)-assisted multicomponent synthesis of heterocycles -- </subfield><subfield code="t">Index</subfield></datafield><datafield tag="506" ind1="0" ind2=" "><subfield code="a">restricted access</subfield><subfield code="u">http://purl.org/coar/access_right/c_16ec</subfield><subfield code="f">online access with authorization</subfield><subfield code="2">star</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Multicomponent synthesis may provide new and green routes for obtaining bioactive heterocycles. These methods produce less organic waste due to no longer removing solvent and other components between reaction steps. It can be applied to the synthesis of heterocycles with reactions such as the Biginelli reaction. This book explores the use of multi-component reactions for various heterocyclic structures with bioactivity.</subfield></datafield><datafield tag="530" ind1=" " ind2=" "><subfield code="a">Issued also in print.</subfield></datafield><datafield tag="538" ind1=" " ind2=" "><subfield code="a">Mode of access: Internet via World Wide Web.</subfield></datafield><datafield tag="546" ind1=" " ind2=" "><subfield code="a">In English.</subfield></datafield><datafield tag="588" ind1="0" ind2=" "><subfield code="a">Description based on online resource; title from PDF title page (publisher's Web site, viewed 06. Mrz 2024)</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Organische Chemie.</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Synthese.</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">grüne Chemie.</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">SCIENCE / Chemistry / General.</subfield><subfield code="2">bisacsh</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">Atom efficiency.</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">Biginelli Reaction.</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">Domino Reactions.</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">Green Chemistry.</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">Green Synthesis.</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">Ionic Liquids.</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">Magnetic Nanocatalysis.</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">Multicomponent Reactions.</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">One-pot Synthesis.</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">Sustainable Developments.</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Amaregouda, Yamanappagouda, </subfield><subfield code="e">contributor.</subfield><subfield code="4">ctb</subfield><subfield code="4">https://id.loc.gov/vocabulary/relators/ctb</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Banerjee, Bubun, </subfield><subfield code="e">contributor.</subfield><subfield code="4">ctb</subfield><subfield code="4">https://id.loc.gov/vocabulary/relators/ctb</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Banerjee, Bubun, </subfield><subfield code="e">editor.</subfield><subfield code="4">edt</subfield><subfield code="4">http://id.loc.gov/vocabulary/relators/edt</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Basu, Basudeb, </subfield><subfield code="e">contributor.</subfield><subfield code="4">ctb</subfield><subfield code="4">https://id.loc.gov/vocabulary/relators/ctb</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Basu, Basudeb, </subfield><subfield code="e">editor.</subfield><subfield code="4">edt</subfield><subfield code="4">http://id.loc.gov/vocabulary/relators/edt</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Biswas, Soumili, </subfield><subfield code="e">contributor.</subfield><subfield code="4">ctb</subfield><subfield code="4">https://id.loc.gov/vocabulary/relators/ctb</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Chakraborti, Asit K., </subfield><subfield code="e">contributor.</subfield><subfield code="4">ctb</subfield><subfield code="4">https://id.loc.gov/vocabulary/relators/ctb</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Das, Asish R., </subfield><subfield code="e">contributor.</subfield><subfield code="4">ctb</subfield><subfield code="4">https://id.loc.gov/vocabulary/relators/ctb</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Dhara, Samiran, </subfield><subfield code="e">contributor.</subfield><subfield code="4">ctb</subfield><subfield code="4">https://id.loc.gov/vocabulary/relators/ctb</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Durga Nageswar, Yadavalli Venkata, </subfield><subfield code="e">contributor.</subfield><subfield code="4">ctb</subfield><subfield code="4">https://id.loc.gov/vocabulary/relators/ctb</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Ghosh, Sujit, </subfield><subfield code="e">contributor.</subfield><subfield code="4">ctb</subfield><subfield code="4">https://id.loc.gov/vocabulary/relators/ctb</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Islam, Saiful, </subfield><subfield code="e">contributor.</subfield><subfield code="4">ctb</subfield><subfield code="4">https://id.loc.gov/vocabulary/relators/ctb</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Kamanna, Kantharaju, </subfield><subfield code="e">contributor.</subfield><subfield code="4">ctb</subfield><subfield code="4">https://id.loc.gov/vocabulary/relators/ctb</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Kamath, Aravind, </subfield><subfield code="e">contributor.</subfield><subfield code="4">ctb</subfield><subfield code="4">https://id.loc.gov/vocabulary/relators/ctb</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Kaur, Manmeet, </subfield><subfield code="e">contributor.</subfield><subfield code="4">ctb</subfield><subfield code="4">https://id.loc.gov/vocabulary/relators/ctb</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Mane, Radhika, </subfield><subfield code="e">contributor.</subfield><subfield code="4">ctb</subfield><subfield code="4">https://id.loc.gov/vocabulary/relators/ctb</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Mathew, Bijoy P., </subfield><subfield code="e">contributor.</subfield><subfield code="4">ctb</subfield><subfield code="4">https://id.loc.gov/vocabulary/relators/ctb</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Nath, Mahendra, </subfield><subfield code="e">contributor.</subfield><subfield code="4">ctb</subfield><subfield code="4">https://id.loc.gov/vocabulary/relators/ctb</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Patel, Divyang M., </subfield><subfield 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N. S., </subfield><subfield code="e">contributor.</subfield><subfield code="4">ctb</subfield><subfield code="4">https://id.loc.gov/vocabulary/relators/ctb</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Sarkar, Anirban, </subfield><subfield code="e">contributor.</subfield><subfield code="4">ctb</subfield><subfield code="4">https://id.loc.gov/vocabulary/relators/ctb</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Scriven, Eric F. 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