SN2′ selective alkylation of allylic chlorides and mesylates with RZnX reagents generated from Grignard reagents, zinc chloride, lithium chloride, and Cu(II)-salts-Reference-Cited by-同舟云学术

SN2′ selective alkylation of allylic chlorides and mesylates with RZnX reagents generated from Grignard reagents, zinc chloride, lithium chloride, and Cu(II)-salts

Published:1993-06 Issue:26 Volume:34 Page:4227-4230
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Fujii Nobutaka,Nakai Kazuo,Habashita Hiromu,Yoshizawa Hidenori,Ibuka Toshiro,Garrido Fabrice,Mann André,Chounan Yukiyasu,Yamamoto Yoshinori

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference27 articles.

1. Highly Stereoselective Synthesis of (E)-Alkene Dipeptide Isosteres as Protease Inhibitors.

2. A new class of proteinase inhibitor. Cyclopropenone-containing inhibitor of papain

3. Highly Selective Synthesis of(E)-Alkene Isosteric Dipeptides With High Optical Purity via RCu(CN)Li·BF3 Mediated Reaction

4. Syn-SN2' pathway in the reaction of certain .gamma.-(mesyloxy) .alpha.,.beta.-enoates with RCu(CN)MgX.BF3 reagents. Importance of MgX and bulky R group upon the diastereoselectivity

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