Enantioselective methodologies using N-carbamoyl-imines
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11310%2F14%3A10195546" target="_blank" >RIV/00216208:11310/14:10195546 - isvavai.cz</a>
Result on the web
<a href="http://dx.doi.org/10.1039/c3cs60321k" target="_blank" >http://dx.doi.org/10.1039/c3cs60321k</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1039/c3cs60321k" target="_blank" >10.1039/c3cs60321k</a>
Alternative languages
Result language
angličtina
Original language name
Enantioselective methodologies using N-carbamoyl-imines
Original language description
Nucleophilic addition to carbon-nitrogen double bonds (imines) represents one of the most common strategies for the synthesis of amine derivatives. In order to circumvent the problem associated with low reactivity of imines in nucleophilic addition, various imines with electron-withdrawing groups at nitrogen have been studied, and many of them were successfully applied in asymmetric methodologies. Especially N-carbamoyl imines were found to be useful in the enantioselective synthesis of various organiccompounds, due to their increased reactivity toward nucleophiles as well as limited difficulties connected with the removal of the carbamoyl moiety in target molecules. The aim of this review is to cover enantioselective methods based on N-carbamoyl imines, focusing on synthetically useful protocols.
Czech name
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Czech description
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Classification
Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
CC - Organic chemistry
OECD FORD branch
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Result continuities
Project
<a href="/en/project/GAP207%2F10%2F0428" target="_blank" >GAP207/10/0428: Enantioselective organocatalytic alpha-alkynylation,alkenylation and arylation of aldehydes and ketones</a><br>
Continuities
Z - Vyzkumny zamer (s odkazem do CEZ)<br>I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Others
Publication year
2014
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Chemical Society Reviews
ISSN
0306-0012
e-ISSN
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Volume of the periodical
43
Issue of the periodical within the volume
2
Country of publishing house
DE - GERMANY
Number of pages
20
Pages from-to
611-630
UT code for WoS article
000329071400009
EID of the result in the Scopus database
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