Enantioselective Synthesis of Cephalimysins B and C

Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14310%2F17%3A00108712" target="_blank" >RIV/00216224:14310/17:00108712 - isvavai.cz</a>
Alternative codes found
RIV/00159816:_____/17:00067028
Result on the web
<a href="https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.6b03373" target="_blank" >https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.6b03373</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1021/acs.orglett.6b03373" target="_blank" >10.1021/acs.orglett.6b03373</a>

Result language
angličtina
Original language name
Enantioselective Synthesis of Cephalimysins B and C
Original language description
The first synthesis of cephalimysins B and C is reported. The route features a Ni(II)-diamine-catalyzed enantioselective conjugate addition of a densely substituted 3(2H)-furanone and an efficient dihydroxylation-lactonization sequence as key steps in the assembly of the spirocyclic core. The fully synthetic strategy is amenable to analog preparation.
Czech name
—
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/LM2015043" target="_blank" >LM2015043: Czech Infrastructure for Integrative Structural Biology</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

Result description