Tuning the Chemoselectivity of the Metathesis Reactions ofN-Substituted 2-Azabicyclo[2.2.1]hept-5-en-3-one-Reference-Cited by-同舟云学术

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Tuning the Chemoselectivity of the Metathesis Reactions ofN-Substituted 2-Azabicyclo[2.2.1]hept-5-en-3-one

Published:2008-08 Issue:23 Volume:2008 Page:3984-3990
ISSN:1434-193X
Container-title:European Journal of Organic Chemistry
language:en
Short-container-title:Eur. J. Org. Chem.

Author:

Aljarilla Ana,Plumet Joaquín

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Reference60 articles.

1. For selected reviews on the synthesis of heterocyclic compounds by using metathesis reactions, see:

2. Synthesis of Oxygen- and Nitrogen-Containing Heterocycles by Ring-Closing Metathesis

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1. Olefin Ring‐Closing Metathesis;Organic Reactions;2016-02

2. Synthesis of Lactams by Metathesis Reactions;Topics in Heterocyclic Chemistry;2015

3. Ring-Rearrangement Metathesis of 7-Azanorbornenes as an Entry to 1-Azabicyclo[n.3.0]alkenones;European Journal of Organic Chemistry;2013-04-18

4. Tandem approaches for the synthesis of functionalized pyrrolidones: efficient routes toward allokainic acid and kainic acid;Tetrahedron Letters;2013-01

5. 2-Azabicyclo[2.2.1]hept-5-en-3-one: Chemical Profile of a Versatile Synthetic Building Block and its Impact on the Development of Therapeutics;Chemical Reviews;2012-06-08

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