Literature DB >> 18396895

Second-generation total synthesis of haterumalide NA using B-alkyl Suzuki-Miyaura coupling.

Ichiro Hayakawa1, Mitsuru Ueda, Masashi Yamaura, Yoichi Ikeda, Yuta Suzuki, Kensaku Yoshizato, Hideo Kigoshi.   

Abstract

Second-generation total synthesis of haterumalide NA, a potent cytotoxic marine macrolide, was achieved by using B-alkyl Suzuki-Miyaura coupling and Nozaki-Hiyama-Kishi coupling as key steps (1.2% in 33 steps). Compared to our first-generation approach, the second-generation synthesis is much improved in the yield of key intermediate.

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Year:  2008        PMID: 18396895     DOI: 10.1021/ol800554f

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  4 in total

Review 1.  Advances in transition metal (Pd, Ni, Fe)-catalyzed cross-coupling reactions using alkyl-organometallics as reaction partners.

Authors:  Ranjan Jana; Tejas P Pathak; Matthew S Sigman
Journal:  Chem Rev       Date:  2011-02-14       Impact factor: 60.622

2.  Enantio- and diastereoselective intermolecular Stetter reaction of glyoxamide and alkylidene ketoamides.

Authors:  Qin Liu; Tomislav Rovis
Journal:  Org Lett       Date:  2009-07-02       Impact factor: 6.005

3.  Total synthesis of haterumalides NA and NC via a chromium-mediated macrocyclization.

Authors:  Jennifer M Schomaker; Babak Borhan
Journal:  J Am Chem Soc       Date:  2008-08-23       Impact factor: 15.419

4.  Chagosensine: A Riddle Wrapped in a Mystery Inside an Enigma.

Authors:  Marc Heinrich; John J Murphy; Marina K Ilg; Aurélien Letort; Jakub T Flasz; Petra Philipps; Alois Fürstner
Journal:  J Am Chem Soc       Date:  2020-03-20       Impact factor: 15.419

  4 in total

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