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Direct addition of alkynes to imines and related C=N electrophiles: A convenient access to propargylamines.
Zani, Lorenzo; Bolm, Carsten.
Affiliation
  • Zani L; Institute of Organic Chemistry, RWTH Aachen University, Landoltweg 1, 52074 Aachen, Germany.
Chem Commun (Camb) ; (41): 4263-75, 2006 Nov 04.
Article in En | MEDLINE | ID: mdl-17047838
Propargylic amines are highly useful building blocks in organic synthesis, and the corresponding structural motif has been found in various natural products and compounds of pharmaceutical relevance. This article provides an overview of the most significant advances in the preparation of propargylic amines via the direct addition of alkynes to imines and related carbon-nitrogen electrophiles in the presence of metal catalysts or promoters.
Subject(s)
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Collection: 01-internacional Database: MEDLINE Main subject: Pargyline / Propylamines / Alkynes / Imines Language: En Journal: Chem Commun (Camb) Journal subject: QUIMICA Year: 2006 Type: Article Affiliation country: Germany
Search on Google
Collection: 01-internacional Database: MEDLINE Main subject: Pargyline / Propylamines / Alkynes / Imines Language: En Journal: Chem Commun (Camb) Journal subject: QUIMICA Year: 2006 Type: Article Affiliation country: Germany