Literature DB >> 11735549

A cobalt-phosphine complex directed Reformatsky approach to a stereospecific synthesis of the dolastatin 10 unit dolaproine (Dap).

G R Pettit1, M P Grealish.   

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Year:  2001        PMID： 11735549     DOI： 10.1021/jo010530t

Source DB:  PubMed          Journal:  J Org Chem        ISSN： 0022-3263            Impact factor:   4.354


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  4 in total

1.  Samarium iodide-mediated Reformatsky reactions for the stereoselective preparation of β-hydroxy-γ-amino acids: synthesis of isostatine and dolaisoleucine.

Authors:  Christopher G Nelson; Terrence R Burke
Journal:  J Org Chem       Date:  2011-12-14       Impact factor: 4.354

2.  Total synthesis of taxane terpenes: cyclase phase.

Authors:  Yoshihiro Ishihara; Abraham Mendoza; Phil S Baran
Journal:  Tetrahedron       Date:  2013-07-08       Impact factor: 2.457

3.  Antineoplastic agents. 592. Highly effective cancer cell growth inhibitory structural modifications of dolastatin 10.

Authors:  George R Pettit; Fiona Hogan; Steven Toms
Journal:  J Nat Prod       Date:  2011-05-02       Impact factor: 4.050

4.  Discovery of Dolastatinol: A Synthetic Analog of Dolastatin 10 and Low Nanomolar Inhibitor of Tubulin Polymerization.

Authors:  Hodaya Gutman; Andrii Bazylevich; Chandrashekhar Prasad; Ortal Dorfman; Arkadi Hesin; Vered Marks; Leonid Patsenker; Gary Gellerman
Journal:  ACS Med Chem Lett       Date:  2021-09-07       Impact factor: 4.632
  4 in total

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