Spongipyran synthetic studies. Evolution of a scalable total synthesis of (+)-spongistatin 1-Reference-Cited by-同舟云学术

Spongipyran synthetic studies. Evolution of a scalable total synthesis of (+)-spongistatin 1

Published:2009-08 Issue:33 Volume:65 Page:6489-6509
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Smith Amos B.,Sfouggatakis Chris,Risatti Christina A.,Sperry Jeffrey B.,Zhu Wenyu,Doughty Victoria A.,Tomioka Takashi,Gotchev Dimitar B.,Bennett Clay S.,Sakamoto Satoshi,Atasoylu Onur,Shirakami Shohei,Bauer David,Takeuchi Makoto,Koyanagi Jyunichi,Sakamoto Yasuharu

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference104 articles.

1. Antineoplastic agents. 257. Isolation and structure of spongistatin 1

2. Altohyrtin A, a potent anti-tumor macrolide from the Okinawan marine sponge Hyrtios altum

3. Bioactive marine metabolites. 48. Cinachyrolide A: a potent cytotoxic macrolide possessing two spiro ketals from marine sponge Cinachyra sp

4. Pettit noted that 400kg of wet sponge yielded only 13.8mg of (+)-spongistatin 1, see: Ref. 1a.

5. Enantioselective Synthesis of Altohyrtin C(Spongistatin 2): Synthesis of the AB- and CD-Spiroketal Subunits

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