An approach to the 3,8-diazabicyclo[3.2.1]octane moiety of naphthyridinomycin and quinocarcin via 1,3-dipolar cycloaddition of photochemically generated azomethine ylides.-Reference-Cited by-同舟云学术

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An approach to the 3,8-diazabicyclo[3.2.1]octane moiety of naphthyridinomycin and quinocarcin via 1,3-dipolar cycloaddition of photochemically generated azomethine ylides.

Published:1988-01 Issue:29 Volume:29 Page:3525-3528
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Garner Philip,Sunitha K.,Shanthilal T.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference30 articles.

1. Naphthyridinomycin;Kluepfel;J. Antibiot.,1975

2. Naphthyridinomycin;Sygusch;Tetrahedron Lett.,1974

3. Errata;Sygusch;Tetrahedron Lett.,1975

4. Cyanocyclin;Zmijewski;J. Antibiot.,1982

5. Cyanocyclin;Hayashi;J. Antibiot.,1982

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