Study towards diversity oriented synthesis of optically active substituted cyclopentane fused carbocyclic and oxacyclic medium-sized rings: Competition between Grubbs-II catalyzed ring closing olefin metathesis and ring closing carbonyl-olefin metathesis

被引:7
|
作者
Chakraborty, P. [1 ]
Roy, S. C. [1 ]
机构
[1] Indian Assoc Cultivat Sci, Dept Organ Chem, Kolkata 700032, India
关键词
Diversity-oriented synthesis; bicyclic frameworks; ring closing metathesis; Grubbs-II catalyst; carbonyl-olefin metathesis; ORGANIC-SYNTHESIS; NATURAL-PRODUCTS; SMALL MOLECULES; ENANTIOSELECTIVE SYNTHESIS; SKELETAL DIVERSITY; ELISABETHIN-A; SCAFFOLDS; ACID; THAPSIGARGINS; CONSTRUCTION;
D O I
10.1007/s12039-016-1197-7
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A study towards diversity-oriented synthesis of optically active cyclopentane fused bicyclic frameworks has been accomplished. The common intermediate was prepared from commercially available starting material (S)-carvone. The observations on competition between Grubbs-II catalyzed ring closing metathesis (RCM) and ring closing carbonyl-olefin metathesis (RCCOM) were the key features of the study.
引用
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页码:1831 / 1840
页数:10
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