Asymmetric Allylic Amination of Morita-Baylis-Hillman Carbonates with Silylated tert-Butylhydroxycarbamate Derivatives

Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11310%2F17%3A10361036" target="_blank" >RIV/00216208:11310/17:10361036 - isvavai.cz</a>
Result on the web
<a href="https://doi.org/10.1002/ejoc.201700222" target="_blank" >https://doi.org/10.1002/ejoc.201700222</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1002/ejoc.201700222" target="_blank" >10.1002/ejoc.201700222</a>

Result language
angličtina
Original language name
Asymmetric Allylic Amination of Morita-Baylis-Hillman Carbonates with Silylated tert-Butylhydroxycarbamate Derivatives
Original language description
The enantioselective amination of Morita-Baylis-Hill-man carbonates with silylated derivatives of tert-butylhydroxy-carbamates using beta-isocupreidine as an organocatalyst was investigated. The corresponding products were obtained in good yields with high enantioselectivities. The scope and limitations of the reported protocol were explored, and representative transformations of the adducts toward heterocyclic compounds were highlighted.
Czech name
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Czech description
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Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
—
OECD FORD branch
10401 - Organic chemistry

Project
<a href="/en/project/GA16-23597S" target="_blank" >GA16-23597S: Organocatalytic Enantioselective Transformations Using Morita-Baylis-Hillman Derivatives and Allenoates (ORG-ETUDA)</a><br>
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Publication year
2017
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

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