Stereoselective Synthesis of 2,6-trans-Tetrahydropyran via Primary Diamine-Catalyzed Oxa-Conjugate Addition Reaction of α,β-Unsaturated Ketone: Total Synthesis of Psymberin-Reference-Cited by-同舟云学术

Stereoselective Synthesis of 2,6-trans-Tetrahydropyran via Primary Diamine-Catalyzed Oxa-Conjugate Addition Reaction of α,β-Unsaturated Ketone: Total Synthesis of Psymberin

Published:2011-10-11 Issue:21 Volume:13 Page:5816-5819
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Byeon Seong Rim¹,Park Heekwang¹,Kim Hyoungsu¹,Hong Jiyong¹

Affiliation:

1. Department of Chemistry, Duke University, Durham, North Carolina 27708, United States, and College of Pharmacy, Ajou University, Suwon 443-749, Korea

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol2024289

Reference87 articles.

1. Antineoplastic Agents. 520. Isolation and Structure of Irciniastatins A and B from the Indo-Pacific Marine Sponge Ircinia ramosa

2. Psymberin, A Potent Sponge-Derived Cytotoxin from Psammocinia Distantly Related to the Pederin Family

3. Synthesis and Complete Stereochemical Assignment of Psymberin/Irciniastatin A

4. A Formal Synthesis of Psymberin

5. The Total Synthesis of Psymberin

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