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NOVEL 2-STEP STEREOSELECTIVE SYNTHESIS OF (E)-ENAMINES AND 1-AMINO-1,3-DIENES FROM TERMINAL ALKYNES

Authors

DOUCET H BRUNEAU C DIXNEUF PH

Citation

H. Doucet et al., NOVEL 2-STEP STEREOSELECTIVE SYNTHESIS OF (E)-ENAMINES AND 1-AMINO-1,3-DIENES FROM TERMINAL ALKYNES, Synlett, (7), 1997, pp. 807

Citations number

Categorie Soggetti

Chemistry Inorganic & Nuclear

Journal title

Synlett → ACNP

ISSN journal

09365214

Issue

Year of publication

1997

Database

ISI

SICI code

0936-5214(1997):7<807:N2SSO(>2.0.ZU;2-A

Abstract

(E)-Enamines and 1-amino-1,3-dienes have been prepared by reaction of secondary amines with alk-1-en-1-yl acetates resulting from the ruthen ium-catalyzed anti-Markovnikov addition of acetic acid to terminal alk ynes and enynes.