Studies on the Synthesis of Nargenicin A1: Highly Stereoselective Synthesis of the Complete Carbon Framework via the Transannular Diels−Alder Reaction of an 18-Membered Macrolide-Reference-Cited by-同舟云学术

Studies on the Synthesis of Nargenicin A1: Highly Stereoselective Synthesis of the Complete Carbon Framework via the Transannular Diels−Alder Reaction of an 18-Membered Macrolide

Published:1996-01-01 Issue:32 Volume:118 Page:7502-7512
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Roush William R.¹,Koyama Kazuo¹,Curtin Michael L.¹,Moriarty Kevin J.¹

Affiliation:

1. Contribution from the Department of Chemistry, Indiana University, Bloomington, Indiana 47405

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja9607796

Reference65 articles.

1. Structure of natural antibiotic CP-47,444

2. Nodusmicin: The structure of a new antibiotic

3. 9-O-esters of nodusmicin.

4. Nargenicin biosynthesis: Late stage oxidations and absolute configuration.

5. Total synthesis of (+)-18-deoxynargenicin A1

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