Synthetic study of arenicolide C: stereoselective synthesis of the C19–C36 segment-Reference-Cited by-同舟云学术

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Synthetic study of arenicolide C: stereoselective synthesis of the C19–C36 segment

Published:2015-12 Issue:48 Volume:56 Page:6693-6695
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Sunagawa Sho,Yamada Haruki,Naito Minako,Yasui Eiko,Mizukami Megumi,Miyashita Masaaki,Nagumo Shinji

Funder

Ministry of Education, Culture, Sports, Science, and Technology

Strategic Research Foundation

Scientific Research

Advanced Promotion Research Program for Education of Graduate School

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference21 articles.

1. Arenicolides A−C, 26-Membered Ring Macrolides from the Marine Actinomycete Salinispora arenicola

2. Stereoselective Synthesis of the C25−C36 Segment of Arenicolides A and B: Determination of the Configuration of the Trisubstituted Epoxide

3. A Stereoselective Synthesis of C26-C36 Fragment of Arenicolide A

4. A Stereoselective Synthesis of C4-C18 Fragment of Arenicolide A

5. Palladium-Catalyzed Stereospecific Substitution of α,β-Unsaturated γ,δ-Epoxy Esters by Alcohols with Double Inversion of Configuration: Synthesis of 4-Alkoxy-5-hydroxy-2-pentenoates

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