Regio- and stereoselectivity in reactions of 2,3-cis- and trans-3-alkyl-2-vinylaziridines with organocopper reagents: Importance of 2,3-cis-stereochemistry in controlling selectivity-Reference-Cited by-同舟云学术

Regio- and stereoselectivity in reactions of 2,3-cis- and trans-3-alkyl-2-vinylaziridines with organocopper reagents: Importance of 2,3-cis-stereochemistry in controlling selectivity

Published:1997-10 Issue:42 Volume:38 Page:7383-7386
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Aoyama Hiroshi,Mimura Norio,Ohno Hiroaki,Ishii Kiyonori,Toda Ayako,Tamamura Hirokazu,Otaka Akira,Fujii Nobutaka,Ibuka Toshiro

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference27 articles.

1. Rearrangements of a 2-vinylaziridine

2. Synthesis of 4-phenylpiperidines by tandem Wittig olefination–aza-Wittig rearrangement of 2-benzoylaziridines

3. Synthesis of new 4-alkylamino-5-methoxy-2H-pyran-2-ones

4. Synthesis and Aza-[2,3]-Wittig Rearrangements of Vinylaziridines: Scope and Limitations

5. Novel Entry to a 3,4-Disubstituted 2-Azetidinone Derivative via Palladium-Assisted Carbonylation of a 2-Substituted 3-Vinylaziridine

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