Efficient synthesis of an enantiomeric pair pinpinidine: An illustration of organochemical carving on the rigid bridged system as the stereochemical tactics-Reference-Cited by-同舟云学术

Efficient synthesis of an enantiomeric pair pinpinidine: An illustration of organochemical carving on the rigid bridged system as the stereochemical tactics

Published:1996-07 Issue:28 Volume:37 Page:4987-4990
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Momose Takefumi,Nishio Takashi,Kirihara Masayuki

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference16 articles.

1. Asymmetric Cleavage of 9-Azabicyclo[3.3.1]nonan-3-one intocis-2,6-Disubstituted Piperidine. A Facile Approach to a Chiral Building Block for Alkaloid Synthesis

2. Total synthesis of (+)-monomorine I via asymmetric .ALPHA.-ketonic cleavage of 8-azabicyclo(3.2.1)octan-3-one.

3. The Tandem Beckmann and Huisgen-White Rearrangement as an Alternative to the Baeyer-Villiger Oxidation of the 9-Azabicyclo[3.3.1]nonan-3-one System: A Facile Route to (±)-Dihydropalustramic Acid

4. The norrish type I photo-cleavage of (+)-2β-ethyl-9-azabicyclo[3.3.1]nonan-3-one: A short, enantioselective formal synthesis of (−)-Indolizidine 223ab

5. Synthetic Studies of Laurencin and Related Compounds. IV. Synthesis ofcis-2-Ethyl-8-formyl-3,4,7,8-dihydro-2H-oxocin-3-one 3-Ethylene Acetal and Related Compounds

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