Synthesis of enantiomerically pure N-(2,3-dihydroxypropyl)arylamides via oxidative esterification

A highly efficient synthesis of enantiomerically pure (S) and (R)-isomers of N-(2,3-dihydroxypropyl)arylamides has been developed with good overall yields in a two step process. The key step involves the ring opening of the chiral epoxide with a nitrogen heterocyclic carbene (NHC) and further rearra...

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Detaylı Bibliyografya
Asıl Yazarlar: Raghunadh, Akula, More, Satish S, Chaitanya, T Krishna, Kumar, Yadla Sateesh, Meruva, Suresh Babu, Rao, L Vaikunta, Kumar, U K Syam
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Beilstein-Institut 2013
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Full Research Paper
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC3817507/
https://ncbi.nlm.nih.gov/pubmed/24204425
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3762/bjoc.9.250
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