Enantiomerically Pure trans-3,4-Disubstituted Tetrahydrothiophenes from Diastereoselective Thiocarbonyl Ylide Addition to Chiral α,β-Unsaturated Amides-Reference-Cited by-同舟云学术

Enantiomerically Pure trans-3,4-Disubstituted Tetrahydrothiophenes from Diastereoselective Thiocarbonyl Ylide Addition to Chiral α,β-Unsaturated Amides

Published:1999-10-10 Issue:10 Volume:1 Page:1667-1669
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Karlsson Staffan¹,Högberg Hans-Erik¹

Affiliation:

1. Department of Chemistry and Process Technology, Mid Sweden University, SE-851 70 Sundsvall, Sweden

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol9910565

Reference9 articles.

1. [3+2]-Cycloaddition of nonstabilized azomethine ylides, part 9: A general approach for the construction of X-azabicyclo[m.2.1]alkanes in optically pure form by asymmetric 1,3-dipolar cycloaddition reactions

2. Karlsson, S.; Han, F.; Högberg, H.E.; Caldirola, P.Tetrahedron: Asymmetry1999,10,2605−2616.

3. Stereospecific synthesis of retronecine by imidate methylide cycloaddition

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