α-Aryl O-Vinyl Carbamates. Tandem Carbolithiation-α-Alkylation and [1,2]-Wittig Rearrangement Reactions

SUPERCHI, Stefano
SOTOMAYOR N.
MIAO G.
JOSEPH B.
CAMPBELL M. G.
SNIECKUS V.

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Publication date

January 1996

DOI

10.1016/0040-4039(96)01315-9

Publisher

Elsevier BV

ISSN

0040-4039

Citation count (estimate)

Abstract

Efficient, one-pot carbolithiation - alpha-alkylation and -[1.2]-Wittig rearrangement processes of alpha-aryl O-vinyl carbamates 1 to branched benzyl O-carbamates 3 and 2-aryl-2-hydroxypropionamides 4, including Naproxen analogues, is describe

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α-Aryl O-Vinyl Carbamates. Tandem Carbolithiation-α-Alkylation and [1,2]-Wittig Rearrangement Reactions

Abstract

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α-Aryl O-Vinyl Carbamates. Tandem Carbolithiation-α-Alkylation and [1,2]-Wittig Rearrangement Reactions

Abstract

Extracted data

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