Mo-catalyzed asymmetric olefin metathesis in target-oriented synthesis: Enantioselective synthesis of (+)-africanol
Author(s) -
Gabriel S. Weatherhead,
G. A. Cortez,
Richard R. Schrock,
Amir H. Hoveyda
Publication year - 2004
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.0307589101
Subject(s) - enantioselective synthesis , metathesis , ring closing metathesis , catalysis , olefin metathesis , tandem , combinatorial chemistry , ring (chemistry) , chemistry , salt metathesis reaction , stereochemistry , organic chemistry , materials science , polymerization , composite material , polymer
Catalytic asymmetric ring-opening metathesis (AROM) provides an efficient method for the synthesis of a variety of optically enriched small organic molecules that cannot be easily prepared by alternative methods. The development of Mo-catalyzed AROM transformations that occur in tandem with ring-closing metathesis are described. The utility of the Mo-catalyzed AROM/ring-closing metathesis is demonstrated through an enantioselective approach to the synthesis of (+)-africanol.
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