Chiral methyllithiums ; the quest for the smallest configurationally stable carbanions / Verf. Dagmar Kapeller
ger: Several heteroatom-substituted chiral [D1]methyllithiums, prepared by transmetalation of the respective tributylstannylmethyl precursors, have been tested towards their microscopic and macroscopic configurational stability. They are versatile tools for stereoselective deuterium labelling and ca...
Saved in:
VerfasserIn: | |
---|---|
Place / Publishing House: | 2008 |
Year of Publication: | 2008 |
Language: | English |
Subjects: | |
Classification: | 35.60 - Metallorganische Verbindungen 35.52 - Präparative Organische Chemie 35.51 - Organische Reaktionen. Stereochemie |
Physical Description: | VI, 231 S.; Ill. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
id |
990001728380504498 |
---|---|
ctrlnum |
AC05036684 (AT-OBV)AC05036684 (DE-599)OBVAC05036684 (EXLNZ-43ACC_NETWORK)990064958830203331 |
collection |
bib_alma |
institution |
YWOAW |
building |
MAG1-3 |
record_format |
marc |
spelling |
Kapeller, Dagmar Christine aut Chiral methyllithiums ; the quest for the smallest configurationally stable carbanions Verf. Dagmar Kapeller 2008 VI, 231 S. Ill. Wien, Univ., Diss., 2008 ger: Several heteroatom-substituted chiral [D1]methyllithiums, prepared by transmetalation of the respective tributylstannylmethyl precursors, have been tested towards their microscopic and macroscopic configurational stability. They are versatile tools for stereoselective deuterium labelling and can be utilised to elucidate reaction mechanisms of biosynthetic or biodegradative pathways. Microscopically, silyloxymethyllithiums underwent smooth retro-Brook rearrangements under complete retention of configuration from 78 °C up to eng: Mehrere Heteroatom-substituierte chirale [D1]Methyllithium-Verbindungen, gewonnen durch Transmetallierung der entsprechenden Tributylstannylmethyl-Vorläufer, sind auf ihre mikroskopisch und makroskopisch konfigurative Stabilität überprüft worden. Diese Spezies sind vielfältig anwendbare Werkzeuge zur stereoselektiven Deuterium-Markierung und können zur Bestimmung sowohl von Reaktionsmechanismen, als auch von Biosynthese- oder Biodegradationswegen verwendet werden.<br />Mikroskopisch gingen Silyloxymethyllithium-Verbindungen eine glatte retro-Brook-Umlagerung zu alpha-Silylalkoholen unter Retention der Konfiguration von 78 °C bis Lithiumorganische Verbindungen s (DE-588)4132581-3 Carbanion s (DE-588)4147276-7 Chiralität Chemie s (DE-588)4147732-7 Stabilität s (DE-588)4056693-6 AT-OBV UBWSCK YWOAW MAG1-3 36792-C.Stip. 2213683630004498 |
language |
English |
format |
Thesis Book |
author |
Kapeller, Dagmar Christine |
spellingShingle |
Kapeller, Dagmar Christine Chiral methyllithiums ; the quest for the smallest configurationally stable carbanions Lithiumorganische Verbindungen (DE-588)4132581-3 Carbanion (DE-588)4147276-7 Chiralität (DE-588)4147732-7 Stabilität (DE-588)4056693-6 |
author_facet |
Kapeller, Dagmar Christine |
author_variant |
d c k dc dck |
author_role |
VerfasserIn |
author_sort |
Kapeller, Dagmar Christine |
title |
Chiral methyllithiums ; the quest for the smallest configurationally stable carbanions |
title_full |
Chiral methyllithiums ; the quest for the smallest configurationally stable carbanions Verf. Dagmar Kapeller |
title_fullStr |
Chiral methyllithiums ; the quest for the smallest configurationally stable carbanions Verf. Dagmar Kapeller |
title_full_unstemmed |
Chiral methyllithiums ; the quest for the smallest configurationally stable carbanions Verf. Dagmar Kapeller |
title_auth |
Chiral methyllithiums ; the quest for the smallest configurationally stable carbanions |
title_new |
Chiral methyllithiums ; the quest for the smallest configurationally stable carbanions |
title_sort |
chiral methyllithiums ; the quest for the smallest configurationally stable carbanions |
publishDate |
2008 |
physical |
VI, 231 S. Ill. |
callnumber-raw |
36792-C.Stip. |
callnumber-search |
36792-C.Stip. |
topic |
Lithiumorganische Verbindungen (DE-588)4132581-3 Carbanion (DE-588)4147276-7 Chiralität (DE-588)4147732-7 Stabilität (DE-588)4056693-6 |
topic_facet |
Lithiumorganische Verbindungen Carbanion Chiralität Stabilität |
illustrated |
Illustrated |
work_keys_str_mv |
AT kapellerdagmarchristine chiralmethyllithiumsthequestforthesmallestconfigurationallystablecarbanions |
status_str |
n |
ids_txt_mv |
(AT-OBV)AC05036684 (DE-599)OBVAC05036684 (EXLNZ-43ACC_NETWORK)990064958830203331 |
hol852bOwn_txt_mv |
YWOAW |
hol852hSignatur_txt_mv |
36792-C.Stip. |
hol852cSonderstandort_txt_mv |
MAG1-3 |
itmData_txt_mv |
2008-11-24 01:00:00 Europe/Vienna |
barcode_str_mv |
+YW12699205 |
callnumbers_txt_mv |
36792-C.Stip. |
inventoryNumbers_str_mv |
36792-C.Stip. |
materialTypes_str_mv |
BOOK |
permanentLibraries_str_mv |
YWOAW |
permanentLocations_str_mv |
MAG1-3 |
inventoryDates_str_mv |
20081124 |
createdDates_str_mv |
2008-11-24 01:00:00 Europe/Vienna |
holdingIds_str_mv |
2213683630004498 |
is_hierarchy_id |
AC05036684 |
is_hierarchy_title |
Chiral methyllithiums ; the quest for the smallest configurationally stable carbanions |
basiskl_str_mv |
35.60 - Metallorganische Verbindungen 35.52 - Präparative Organische Chemie 35.51 - Organische Reaktionen. Stereochemie |
basiskl_txtF_mv |
35.60 - Metallorganische Verbindungen 35.52 - Präparative Organische Chemie 35.51 - Organische Reaktionen. Stereochemie |
_version_ |
1796651486108712962 |
fullrecord |
<?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>02720nam#a2200457#c#4500</leader><controlfield tag="001">990001728380504498</controlfield><controlfield tag="005">20230302184201.0</controlfield><controlfield tag="007">tu</controlfield><controlfield tag="008">080213|2008####|||######m####|||#|#eng#c</controlfield><controlfield tag="009">AC05036684</controlfield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(AT-OBV)AC05036684</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-599)OBVAC05036684</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(EXLNZ-43ACC_NETWORK)990064958830203331</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">UBW</subfield><subfield code="b">ger</subfield><subfield code="c">OPUS</subfield><subfield code="d">AT-OBV</subfield><subfield code="e">rakwb</subfield></datafield><datafield tag="041" ind1=" " ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="044" ind1=" " ind2=" "><subfield code="c">XA-AT</subfield></datafield><datafield tag="084" ind1=" " ind2=" "><subfield code="a">35.60</subfield><subfield code="2">bkl</subfield></datafield><datafield tag="084" ind1=" " ind2=" "><subfield code="a">35.52</subfield><subfield code="2">bkl</subfield></datafield><datafield tag="084" ind1=" " ind2=" "><subfield code="a">35.51</subfield><subfield code="2">bkl</subfield></datafield><datafield tag="100" ind1="1" ind2=" "><subfield code="a">Kapeller, Dagmar Christine</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Chiral methyllithiums ; the quest for the smallest configurationally stable carbanions</subfield><subfield code="c">Verf. Dagmar Kapeller</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">2008</subfield></datafield><datafield tag="300" ind1=" " ind2=" "><subfield code="a">VI, 231 S.</subfield><subfield code="b">Ill.</subfield></datafield><datafield tag="502" ind1=" " ind2=" "><subfield code="a">Wien, Univ., Diss., 2008</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">ger: Several heteroatom-substituted chiral [D1]methyllithiums, prepared by transmetalation of the respective tributylstannylmethyl precursors, have been tested towards their microscopic and macroscopic configurational stability. They are versatile tools for stereoselective deuterium labelling and can be utilised to elucidate reaction mechanisms of biosynthetic or biodegradative pathways. Microscopically, silyloxymethyllithiums underwent smooth retro-Brook rearrangements under complete retention of configuration from 78 °C up to</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">eng: Mehrere Heteroatom-substituierte chirale [D1]Methyllithium-Verbindungen, gewonnen durch Transmetallierung der entsprechenden Tributylstannylmethyl-Vorläufer, sind auf ihre mikroskopisch und makroskopisch konfigurative Stabilität überprüft worden. Diese Spezies sind vielfältig anwendbare Werkzeuge zur stereoselektiven Deuterium-Markierung und können zur Bestimmung sowohl von Reaktionsmechanismen, als auch von Biosynthese- oder Biodegradationswegen verwendet werden.<br />Mikroskopisch gingen Silyloxymethyllithium-Verbindungen eine glatte retro-Brook-Umlagerung zu alpha-Silylalkoholen unter Retention der Konfiguration von 78 °C bis</subfield></datafield><datafield tag="689" ind1="0" ind2="0"><subfield code="a">Lithiumorganische Verbindungen</subfield><subfield code="D">s</subfield><subfield code="0">(DE-588)4132581-3</subfield></datafield><datafield tag="689" ind1="0" ind2="1"><subfield code="a">Carbanion</subfield><subfield code="D">s</subfield><subfield code="0">(DE-588)4147276-7</subfield></datafield><datafield tag="689" ind1="0" ind2="2"><subfield code="a">Chiralität</subfield><subfield code="g">Chemie</subfield><subfield code="D">s</subfield><subfield code="0">(DE-588)4147732-7</subfield></datafield><datafield tag="689" ind1="0" ind2="3"><subfield code="a">Stabilität</subfield><subfield code="D">s</subfield><subfield code="0">(DE-588)4056693-6</subfield></datafield><datafield tag="689" ind1="0" ind2=" "><subfield code="5">AT-OBV</subfield><subfield code="5">UBWSCK</subfield></datafield><datafield tag="970" ind1="1" ind2=" "><subfield code="c">30</subfield></datafield><datafield tag="970" ind1="2" ind2=" "><subfield code="d">HS-DISS</subfield></datafield><datafield tag="970" ind1="0" ind2=" "><subfield code="a">OPUS10965</subfield></datafield><datafield tag="971" ind1="0" ind2=" "><subfield code="a">Hammerschmidt, Friedrich</subfield></datafield><datafield tag="971" ind1="1" ind2=" "><subfield code="a">Gärtner, Peter</subfield></datafield><datafield tag="971" ind1="1" ind2=" "><subfield code="a">Hoffmann, Reinhard</subfield></datafield><datafield tag="971" ind1="3" ind2=" "><subfield code="a">2008-02</subfield></datafield><datafield tag="971" ind1="4" ind2=" "><subfield code="a">Dr. rer. nat.</subfield></datafield><datafield tag="971" ind1="5" ind2=" "><subfield code="a">Universität Wien</subfield><subfield code="b">Fakultät für Chemie</subfield><subfield code="c">Institut für Organische Chemie</subfield></datafield><datafield tag="971" ind1="8" ind2=" "><subfield code="a">Organolithium-Verbindungen / konfigurative Stabilität / Carbanionen / Umlagerungen / Chiralität</subfield></datafield><datafield tag="971" ind1="9" ind2=" "><subfield code="a">organolithiums / configurational stability / carbanions / rearrangements / chirality</subfield></datafield><datafield tag="ADM" ind1=" " ind2=" "><subfield code="b">2024-03-18 00:52:01 Europe/Vienna</subfield><subfield code="d">20</subfield><subfield code="f">System</subfield><subfield code="c">marc21</subfield><subfield code="a">2018-12-24 05:17:36 Europe/Vienna</subfield><subfield code="g">false</subfield></datafield><datafield tag="HOL" ind1="8" ind2=" "><subfield code="b">YWOAW</subfield><subfield code="h"> 36792-C.Stip. </subfield><subfield code="c">MAG1-3</subfield><subfield code="8">2213683630004498</subfield></datafield><datafield tag="852" ind1="8" ind2=" "><subfield code="b">YWOAW</subfield><subfield code="c">MAG1-3</subfield><subfield code="h"> 36792-C.Stip. </subfield><subfield code="8">2213683630004498</subfield></datafield><datafield tag="ITM" ind1=" " ind2=" "><subfield code="9">2213683630004498</subfield><subfield code="e">1</subfield><subfield code="m">BOOK</subfield><subfield code="b">+YW12699205</subfield><subfield code="i">36792-C.Stip.</subfield><subfield code="2">MAG1-3</subfield><subfield code="o">20081124</subfield><subfield code="8">2313683610004498</subfield><subfield code="f">02</subfield><subfield code="p">2008-11-24 01:00:00 Europe/Vienna</subfield><subfield code="h">36792-C.Stip.</subfield><subfield code="1">YWOAW</subfield><subfield code="q">2022-06-09 11:14:08 Europe/Vienna</subfield></datafield></record></collection> |