Enantiospecific preparation of [(2r,6s)-endo]-5-aza-1,10,10-trimethyl-3-oxatricyclo[5.2.1.02,6]decan-4-one by a nitrene-mediated route from [(1s)-endo]-(−)-borneol and its utility as a chiral auxiliary in some asymmetric transformations-Reference-Cited by-同舟云学术

Enantiospecific preparation of [(2r,6s)-endo]-5-aza-1,10,10-trimethyl-3-oxatricyclo[5.2.1.02,6]decan-4-one by a nitrene-mediated route from [(1s)-endo]-(−)-borneol and its utility as a chiral auxiliary in some asymmetric transformations

Published:1992-01 Issue:37 Volume:48 Page:7979-8006
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Banks Malcolm R.,Blake Alexander J.,Cadogan J.I.G.,Dawson Ian M.,Gosney Ian,Grant Keith J.,Gaur Suneel,Hodgson Philip K.G.,Knight Kevin S.,Smith Glen W.,Stevenson (nee Thomson) Dian E.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference33 articles.

1. Stereo and regioselective openings of chiral 2,3-epoxy alcohols. Versatile routes to optically pure natural products and drugs. Unusual kinetic resolutions

2. The Absolute Configurations of 2-Phenylaziridine and Its Derivatives

3. Addition of iodine isocyanate to olefins. Scope and synthetic utility

4. Chiral aziridination of alkenes

5. Chiral aziridination of alkenes: oxidation of 3-amino-2-(1,2,2-trimethyl)propylquinazolin-4(3H)-one in the presence of alkenes

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