Literature DB >> 15901178

A sequential palladium-catalyzed alder-ene-reductive amination reaction.

Christoph J Kressierer1, Thomas J J Müller.   

Abstract

[reaction: see text]. Alkyne allyl alcohols are readily transformed into beta-amino ethyl alkylidene tetrahydrofurans or beta-amino ethyl alkylidene pyrrolidines in a Pd-catalyzed cycloisomerization-reductive amination sequence with remarkable chemoselectivity leaving benzyl groups and trisubstituted double bonds intact.

Entities:  

Year:  2005        PMID： 15901178     DOI： 10.1021/ol050674k

Source DB:  PubMed          Journal:  Org Lett        ISSN： 1523-7052            Impact factor:   6.005


  1 in total

1.  On the Origin of the Promoting Effect Exerted by Magnesium in the ZnCl2-Catalyzed Synthesis of N,N-Diisopropylethylamine.

Authors:  Zeng Hong; Jiancheng Ruan; Xinzhi Chen; Chao Qian; Xin Ge; Shaodong Zhou
Journal:  ACS Omega       Date:  2020-11-11
  1 in total

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