Synthetic Studies of Antitumor Macrolide Rhizoxin: Stereoselective Syntheses of the C(1)−C(9) and C(12)−C(26) Subunits-Reference-Cited by-同舟云学术

Synthetic Studies of Antitumor Macrolide Rhizoxin: Stereoselective Syntheses of the C(1)−C(9) and C(12)−C(26) Subunits

Published:1998-09-05 Issue:20 Volume:63 Page:6952-6967
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Burke Steven D.¹,Hong Jian¹,Lennox Joseph R.¹,Mongin Andrew P.¹

Affiliation:

1. Department of Chemistry, University of WisconsinMadison, Madison, Wisconsin 53706, and Department of Chemical Sciences, Wyeth−Ayerst Research, Princeton, New Jersey 08543-8000

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo980754k

Reference121 articles.

1. Studies on macrocyclic lactone antibiotics. VII Structure of a phytotoxin "rhizoxin" produced by Rhizopus chinensis.

2. Studies on macrocyclic lactone antibiotics. IX. Novel macrolides from the fungus Rhizopus chinensis: Precursors of rhizoxin.

3. A new antitumor complex, WF-1360, WF-1360A, B, C, D, E and F.

4. Studies on macrocyclic lactone antibiotics. XI. Anti-mitotic and anti-tubulin activity of new antitumor antibiotics, rhizoxin and its homologues.

5. Studies on macrocyclic lactone antibiotics. VIII. Absolute structures of rhizoxin and a related compound.

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