“Endo” and “Exo” Bicyclo[4.2.0]-octadiene Isomers from the Electrocyclization of Fully Substituted Tetraene Models for SNF 4435C and D. Control of Stereochemistry by Choice of a Functionalized Substituent-Reference-Cited by-同舟云学术

“Endo” and “Exo” Bicyclo[4.2.0]-octadiene Isomers from the Electrocyclization of Fully Substituted Tetraene Models for SNF 4435C and D. Control of Stereochemistry by Choice of a Functionalized Substituent

Published:2003-12-17 Issue:2 Volume:6 Page:161-164
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Parker Kathlyn A.¹,Lim Yeon-Hee¹

Affiliation:

1. Department of Chemistry, State University of New York at Stony Brook, Stony Brook, New York, 11794-3400

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol036048%2B

Reference13 articles.

1. SNF4435C and D, Novel Immunosuppressants Produced by a Strain of Streptomyces spectabilis. I. Taxonomy, Fermentation, Isolation and Biological Activities.

2. SNF4435C and D, Novel Immunosuppressants Produced by a Strain of Streptomyces spectabilis. III. Immunosuppressive Efficacy.

3. Reversal of Multidrug Resistance by Novel Nitrophenyl Pyrones, SNF4435C and D

4. SNF4435C and D, Novel Immunosuppressants Produced by a Strain of Streptomyces spectabilis. II. Structure Elucidation.

5. Synthetic Studies toward SNF4435 C and SNF4435 D

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