Literature DB >> 12678763

Chemistry of potent anti-cancer compounds, amphidinolides.

T K Chakraborty1, S Das.   

Abstract

Amphidinolides A-V represent a family of cytotoxic marine natural products with diverse structural features and pronounced biological activities. Kobayashi and his research group have been reporting over the years the discoveries of these remarkable molecules, one after another, since 1986 when the first report of the series appeared. Thanks to their perseverance and painstaking research, the family is still expanding. The unique structural features and biological activity profiles of these macrolides have obviously attracted the attention of organic chemists worldwide. The total syntheses of three members of the family, amphidinolides J, K and P, have already been achieved. This review tries to chronicle the fascinating chemistries of amphidinolides, studies on the syntheses of some of these molecules and their biological activity profiles.

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Year:  2001        PMID: 12678763     DOI: 10.2174/1568011013354660

Source DB:  PubMed          Journal:  Curr Med Chem Anticancer Agents        ISSN: 1568-0118


  13 in total

1.  Synthetic studies on amphidinolide B1.

Authors:  Amit K Mandal; John S Schneekloth; Kouji Kuramochi; Craig M Crews
Journal:  Org Lett       Date:  2006-02-02       Impact factor: 6.005

2.  Synthesis of the C3-C18 fragment of amphidinolides G and H.

Authors:  Andreas F Petri; John S Schneekloth; Amit K Mandal; Craig M Crews
Journal:  Org Lett       Date:  2007-07-07       Impact factor: 6.005

3.  Amphidinolide B: total synthesis, structural investigation, and biological evaluation.

Authors:  Liang Lu; Wei Zhang; Sangkil Nam; David A Horne; Richard Jove; Rich G Carter
Journal:  J Org Chem       Date:  2013-02-13       Impact factor: 4.354

4.  Synthesis of 2-epi-amphidinolide E: an unexpected and highly selective C(2)inversion during an esterification reaction.

Authors:  Porino Va; William R Roush
Journal:  Org Lett       Date:  2007-01-18       Impact factor: 6.005

5.  Stereoselective assembly of a 1,3-diene via coupling between an allenic acetate and a (B)-alkylborane: synthetic studies on amphidinolide B1.

Authors:  Amit K Mandal; John S Schneekloth; Craig M Crews
Journal:  Org Lett       Date:  2005-08-18       Impact factor: 6.005

6.  Total syntheses of amphidinolides T1 and T4 via catalytic, stereoselective, reductive macrocyclizations.

Authors:  Elizabeth A Colby; Karen C O'Brien; Timothy F Jamison
Journal:  J Am Chem Soc       Date:  2005-03-30       Impact factor: 15.419

7.  Ru-catalyzed alkene-alkyne coupling. Total synthesis of amphidinolide P.

Authors:  Barry M Trost; Julien P N Papillon; Thomas Nussbaumer
Journal:  J Am Chem Soc       Date:  2005-12-21       Impact factor: 15.419

8.  Stereoselective syntheses of the C(1)-C(9) fragment of amphidinolide C.

Authors:  Robert H Bates; J Brad Shotwell; William R Roush
Journal:  Org Lett       Date:  2008-09-11       Impact factor: 6.005

9.  Studies for the total synthesis of amphidinolide P.

Authors:  David R Williams; Brian J Myers; Liang Mi; Randall J Binder
Journal:  J Org Chem       Date:  2013-04-26       Impact factor: 4.354

10.  Total Synthesis of Amphidinolide E and Amphidinolide E Stereoisomers.

Authors:  Porino Va; William R Roush
Journal:  Tetrahedron       Date:  2007-06-25       Impact factor: 2.457

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