A Novel Skeletal Rearrangement of 2-Azabicyclo[2.2.1]hept-5-ene-3-carboxylic Acid Derivatives into 2-Oxabicyclo[3.3.0]-oct-7-en-3-ones under Acidic Conditions-Reference-Cited by-同舟云学术

A Novel Skeletal Rearrangement of 2-Azabicyclo[2.2.1]hept-5-ene-3-carboxylic Acid Derivatives into 2-Oxabicyclo[3.3.0]-oct-7-en-3-ones under Acidic Conditions

Published:1992-01 Issue:1 Volume:65 Page:61-65
ISSN:0009-2673
Container-title:Bulletin of the Chemical Society of Japan
language:en
Short-container-title:BCSJ

Author:

Kobayashi Tomoshige,Ono Katsuhiko,Kato Hiroshi

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Link

https://www.jstage.jst.go.jp/article/bcsj/65/1/65_1_61/_pdf

Reference29 articles.

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2. Synthetic aspects of diels-alder cycloadditions with heterodienophiles

3. Aza Diels-Alder reactions in aqueous solution: cyclocondensation of dienes with simple iminium salts generated under Mannich conditions

4. Aza Diels-Alder reactions in water: Cyclocondensation of C-acyl iminium ions with cyclopentadiene

5. Stereoselective synthesis of pipecolic acid derivatives using aza-diels-alder reactions

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