Modern Strategies for Heterocycle Synthesis

Heterocycles feature widely in natural products, agrochemicals, pharmaceuticals and dyes, and their synthesis is of great interest to synthetic chemists in both academia and industry. The contributions of recent applications of new methodologies in C–H activation, photoredox chemistry, cross-couplin...

Full description

Saved in:
Bibliographic Details
Sonstige:
Year of Publication:2021
Language:English
Physical Description:1 electronic resource (372 p.)
Tags: Add Tag
No Tags, Be the first to tag this record!
id 993545553404498
ctrlnum (CKB)5400000000043577
(oapen)https://directory.doabooks.org/handle/20.500.12854/68487
(EXLCZ)995400000000043577
collection bib_alma
record_format marc
spelling Favi, Gianfranco edt
Modern Strategies for Heterocycle Synthesis
Basel, Switzerland MDPI - Multidisciplinary Digital Publishing Institute 2021
1 electronic resource (372 p.)
text txt rdacontent
computer c rdamedia
online resource cr rdacarrier
Heterocycles feature widely in natural products, agrochemicals, pharmaceuticals and dyes, and their synthesis is of great interest to synthetic chemists in both academia and industry. The contributions of recent applications of new methodologies in C–H activation, photoredox chemistry, cross-coupling strategies, borrowing hydrogen catalysis, multicomponent and solvent-free reactions, regio- and stereoselective syntheses, as well as other new, attractive approaches for the construction of heterocyclic scaffolds are of great interest. This Special Issue is dedicated to featuring the latest research that is ongoing in the field of heterocyclic synthesis. It is expected that most submissions will focus on five- and six-membered oxygen and nitrogen-containing heterocycles, but structures incorporating other rings/heteroatoms will also be considered. Original research (communications, full papers and reviews) that discusses innovative methodologies for assembling heterocycles with potential application in materials, catalysis and medicine are therefore welcome.
English
Medicine bicssc
amine nucleophiles
alkynoic acids
cascade reaction
gold catalysis
fused N-heterocycles
solid-phase synthesis
ketone
traceless synthesis
natural products
enol ethers
photocatalysis
photoredox
visible-light-induced catalysis
photoredox cyclization
organic dyes
heterocycles
dihydrocoumarins
synthesis
3-trifluoroacetyl coumarins
phenols
antifungal activities
terpyridines
3,2':6',3"-terpyridine
cyclohexanol derivative
condensation
heterocyclic
1,2,3-triazol
triazolylmethyl phosphinate
triazolylmethyl phosphate
copper-catalyzed azide-alkyne cycloaddition
click reaction
azides
cinnolines
triazoles
CuAAC
alkynes
cycloalkynes
Richter cyclization
Suzuki coupling
fluorescence
cytotoxicity
coumarin
pyrazolo[3,4-b]pyridine
silica sulfuric acid
2H-pyran
valence isomerism
1-oxa-triene
dienone
oxa-electrocyclization
Knoevenagel
propargyl Claisen
cycloisomerization
asymmetric dimeric β-carboline
acylhydrazone group
cytotoxic
antitumor
structure-activity relationship
γ-lactam
pyrrolidones
multicomponent reactions
organocatalysis
pyridine
CF3CO-acetylenes
1,3-oxazines
fluorinated heterocycles
saturated oxygen heterocycles
cyclic ethers
total synthesis
multicomponent reaction
α-halohydrazones
Staudinger reaction
aza-Wittig
1H-imidazole-2(3H)-thione
2H-imidazo[2,1-b][1,3,4]thiadiazine
purine
nucleobase
aromatic substitution
arylation
fluoroalcohol
α-chloroglycinates
5-acylamino-1,3-thiazoles
Hantzsch reaction
TMSBr
propargylic alcohols
cascade cyclization
4-bromo quinolines
synthesis of benzofurans
intra-molecular approach
inter-molecular approach
3-0365-0340-4
3-0365-0341-2
Favi, Gianfranco oth
language English
format eBook
author2 Favi, Gianfranco
author_facet Favi, Gianfranco
author2_variant g f gf
author2_role Sonstige
title Modern Strategies for Heterocycle Synthesis
spellingShingle Modern Strategies for Heterocycle Synthesis
title_full Modern Strategies for Heterocycle Synthesis
title_fullStr Modern Strategies for Heterocycle Synthesis
title_full_unstemmed Modern Strategies for Heterocycle Synthesis
title_auth Modern Strategies for Heterocycle Synthesis
title_new Modern Strategies for Heterocycle Synthesis
title_sort modern strategies for heterocycle synthesis
publisher MDPI - Multidisciplinary Digital Publishing Institute
publishDate 2021
physical 1 electronic resource (372 p.)
isbn 3-0365-0340-4
3-0365-0341-2
illustrated Not Illustrated
work_keys_str_mv AT favigianfranco modernstrategiesforheterocyclesynthesis
status_str n
ids_txt_mv (CKB)5400000000043577
(oapen)https://directory.doabooks.org/handle/20.500.12854/68487
(EXLCZ)995400000000043577
carrierType_str_mv cr
is_hierarchy_title Modern Strategies for Heterocycle Synthesis
author2_original_writing_str_mv noLinkedField
_version_ 1787548474717241344
fullrecord <?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>04976nam-a2201357z--4500</leader><controlfield tag="001">993545553404498</controlfield><controlfield tag="005">20231214133337.0</controlfield><controlfield tag="006">m o d </controlfield><controlfield tag="007">cr|mn|---annan</controlfield><controlfield tag="008">202105s2021 xx |||||o ||| 0|eng d</controlfield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(CKB)5400000000043577</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(oapen)https://directory.doabooks.org/handle/20.500.12854/68487</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(EXLCZ)995400000000043577</subfield></datafield><datafield tag="041" ind1="0" ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="100" ind1="1" ind2=" "><subfield code="a">Favi, Gianfranco</subfield><subfield code="4">edt</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Modern Strategies for Heterocycle Synthesis</subfield></datafield><datafield tag="260" ind1=" " ind2=" "><subfield code="a">Basel, Switzerland</subfield><subfield code="b">MDPI - Multidisciplinary Digital Publishing Institute</subfield><subfield code="c">2021</subfield></datafield><datafield tag="300" ind1=" " ind2=" "><subfield code="a">1 electronic resource (372 p.)</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">text</subfield><subfield code="b">txt</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">computer</subfield><subfield code="b">c</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">online resource</subfield><subfield code="b">cr</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Heterocycles feature widely in natural products, agrochemicals, pharmaceuticals and dyes, and their synthesis is of great interest to synthetic chemists in both academia and industry. The contributions of recent applications of new methodologies in C–H activation, photoredox chemistry, cross-coupling strategies, borrowing hydrogen catalysis, multicomponent and solvent-free reactions, regio- and stereoselective syntheses, as well as other new, attractive approaches for the construction of heterocyclic scaffolds are of great interest. This Special Issue is dedicated to featuring the latest research that is ongoing in the field of heterocyclic synthesis. It is expected that most submissions will focus on five- and six-membered oxygen and nitrogen-containing heterocycles, but structures incorporating other rings/heteroatoms will also be considered. Original research (communications, full papers and reviews) that discusses innovative methodologies for assembling heterocycles with potential application in materials, catalysis and medicine are therefore welcome.</subfield></datafield><datafield tag="546" ind1=" " ind2=" "><subfield code="a">English</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Medicine</subfield><subfield code="2">bicssc</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">amine nucleophiles</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">alkynoic acids</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">cascade reaction</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">gold catalysis</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">fused N-heterocycles</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">solid-phase synthesis</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">ketone</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">traceless synthesis</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">natural products</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">enol ethers</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">photocatalysis</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">photoredox</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">visible-light-induced catalysis</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">photoredox cyclization</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">organic dyes</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">heterocycles</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">dihydrocoumarins</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">synthesis</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">3-trifluoroacetyl coumarins</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">phenols</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">antifungal activities</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">terpyridines</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">3,2':6',3"-terpyridine</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">cyclohexanol derivative</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">condensation</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">heterocyclic</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">1,2,3-triazol</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">triazolylmethyl phosphinate</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">triazolylmethyl phosphate</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">copper-catalyzed azide-alkyne cycloaddition</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">click reaction</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">azides</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">cinnolines</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">triazoles</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">CuAAC</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">alkynes</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">cycloalkynes</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">Richter cyclization</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">Suzuki coupling</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">fluorescence</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">cytotoxicity</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">coumarin</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">pyrazolo[3,4-b]pyridine</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">silica sulfuric acid</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">2H-pyran</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">valence isomerism</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">1-oxa-triene</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">dienone</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">oxa-electrocyclization</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">Knoevenagel</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">propargyl Claisen</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">cycloisomerization</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">asymmetric dimeric β-carboline</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">acylhydrazone group</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">cytotoxic</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">antitumor</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">structure-activity relationship</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">γ-lactam</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">pyrrolidones</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">multicomponent reactions</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">organocatalysis</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">pyridine</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">CF3CO-acetylenes</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">1,3-oxazines</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">fluorinated heterocycles</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">saturated oxygen heterocycles</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">cyclic ethers</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">total synthesis</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">multicomponent reaction</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">α-halohydrazones</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">Staudinger reaction</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">aza-Wittig</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">1H-imidazole-2(3H)-thione</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">2H-imidazo[2,1-b][1,3,4]thiadiazine</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">purine</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">nucleobase</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">aromatic substitution</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">arylation</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">fluoroalcohol</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">α-chloroglycinates</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">5-acylamino-1,3-thiazoles</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">Hantzsch reaction</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">TMSBr</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">propargylic alcohols</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">cascade cyclization</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">4-bromo quinolines</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">synthesis of benzofurans</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">intra-molecular approach</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">inter-molecular approach</subfield></datafield><datafield tag="776" ind1=" " ind2=" "><subfield code="z">3-0365-0340-4</subfield></datafield><datafield tag="776" ind1=" " ind2=" "><subfield code="z">3-0365-0341-2</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Favi, Gianfranco</subfield><subfield code="4">oth</subfield></datafield><datafield tag="906" ind1=" " ind2=" "><subfield code="a">BOOK</subfield></datafield><datafield tag="ADM" ind1=" " ind2=" "><subfield code="b">2023-12-15 05:50:53 Europe/Vienna</subfield><subfield code="f">system</subfield><subfield code="c">marc21</subfield><subfield code="a">2022-04-04 09:22:53 Europe/Vienna</subfield><subfield code="g">false</subfield></datafield><datafield tag="AVE" ind1=" " ind2=" "><subfield code="i">DOAB Directory of Open Access Books</subfield><subfield code="P">DOAB Directory of Open Access Books</subfield><subfield code="x">https://eu02.alma.exlibrisgroup.com/view/uresolver/43ACC_OEAW/openurl?u.ignore_date_coverage=true&amp;portfolio_pid=5337978540004498&amp;Force_direct=true</subfield><subfield code="Z">5337978540004498</subfield><subfield code="b">Available</subfield><subfield code="8">5337978540004498</subfield></datafield></record></collection>