| Literature DB >> 23909700 |
Isao Mizota1, Yuri Matsuda, Satoshi Kamimura, Hirotaka Tanaka, Makoto Shimizu.
Abstract
A new synthesis of α-quaternary alkynyl amino esters and allenoates was developed utilizing umpolung N-addition to β,γ-alkynyl α-imino esters followed by regioselective acylation. The reaction exhibits broad substrate generality and unique regioselectivity. Moreover, synthesis of α-quaternary alkynyl amino esters was also carried out via oxidation of the intermediary enolate followed by alkylation.Entities:
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Year: 2013 PMID: 23909700 DOI: 10.1021/ol401934x
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005