The First Successful Base-Promoted Isomerization of Propargyl Amides to Chiral Ynamides. Applications in Ring-Closing Metathesis of Ene−Ynamides and Tandem RCM of Diene−Ynamides-Reference-Cited by-同舟云学术

The First Successful Base-Promoted Isomerization of Propargyl Amides to Chiral Ynamides. Applications in Ring-Closing Metathesis of Ene−Ynamides and Tandem RCM of Diene−Ynamides

Published:2002-06-13 Issue:14 Volume:4 Page:2417-2420
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Huang Jian¹,Xiong Hui¹,Hsung Richard P.¹,Rameshkumar C.¹,Mulder Jason A.¹,Grebe Tyler P.¹

Affiliation:

1. Department of Chemistry, University of Minnesota, Minneapolis, Minnesota 55455

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol020097p

Reference27 articles.

1. Recent advances in the chemistry of ynamines and ynamides

2. The Synthesis and Chemoselective Reactivity of 3-Aminocyclopentadienones

3. Conjugate Addition of Lithiated (S)-4-Isopropyl-3- [(methylthio)methyl]-5,5-diphenyloxazolidin-2-one to Cinnamoyl Derivatives: Preparation of Enantiomerically Pure 1,4-Diols

4. The First Stereoselective Ficini−Claisen Rearrangement Using Chiral Ynamides

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