Development of Catalytic Asymmetric Intramolecular Cyclopropanation of α-Diazo-β-Keto Sulfones and Applications to Natural Product Synthesis

被引:48
作者
Honma, Masahiro [1 ]
Takeda, Hiroyuki [1 ]
Takano, Masashi [1 ]
Nakada, Masahisa [1 ]
机构
[1] Waseda Univ, Fac Sci & Engn, Dept Chem & Biochem, Shinjuku Ku, Tokyo 1698555, Japan
关键词
asymmetric catalysis; carbene complexes; diazo compounds; natural products; sulfones; ENANTIOSELECTIVE TOTAL-SYNTHESIS; (+/-)-ALLOCYATHIN B-2; CYATHIN DITERPENES; COMPLEXES; OXIDATION; DERIVATIVES; LITHIUM; DEHYDROGENATION; CONSTRUCTION; TEMPERATURE;
D O I
10.1055/s-0029-1217363
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The catalytic asymmetric intramolecular cyclopropanation (CAIMCP) of alpha-diazo-beta-keto sulfones developed in our laboratory and applications to the total synthesis of natural products are described. CAIMCP features(a) a wide applicability, not only to the preparation of bicyclo[n.1.0]alkanes and tricyclo[4.n.0.0]alkenes, but also to the enantioselective total synthesis of natural products, (b) the formation of highly crystalline products, which facilitate the production of enantiomerically pure synthetic intermediates, and (c) the generation of products with a variety of functionalities, Such as cyclopropane, ketone, and sulfone, beneficial to the total synthesis of natural products.
引用
收藏
页码:1695 / 1712
页数:18
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