[3 + 2]-Cycloaddition of Nonstabilized Azomethine Ylides. 10. An Efficient Strategy for the Construction of x-Azatricyclo[m.n.0.0a,b]alkanes by Intramolecular Cycloaddition of Cyclic Azomethine Ylide-Reference-Cited by-同舟云学术

[3 + 2]-Cycloaddition of Nonstabilized Azomethine Ylides. 10. An Efficient Strategy for the Construction of x-Azatricyclo[m.n.0.0a,b]alkanes by Intramolecular Cycloaddition of Cyclic Azomethine Ylide

Published:2000-06-30 Issue:15 Volume:2 Page:2299-2301
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Pandey Ganesh¹,Sahoo Akhila K.¹,Bagul Trusar D.¹

Affiliation:

1. Division of Organic Chemistry (Synthesis), National Chemical Laboratory, Pune 411 008, India

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol006070s

Reference42 articles.

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4. (a) Wade, P. A.Intramolecular 1,3-Dipolar Cycloadditions In ComprehensiveOrganic Synthesis; Trost, B. M., Fleming, I., Eds.; Pergamon: London, 1991; Vol. 4, p 1111.

5. Intramolecular dipolar cycloaddition reactions with azomethine ylides

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