MARINE NATURAL PRODUCTS;
D-PANTOLACTONE;
D-ISOBUTYL LACTATE;
DIASTEREOSELECTIVITY IN ALLYLATION;
ALDOL AND REDUCTION REACTIONS;
D O I:
暂无
中图分类号:
O62 [有机化学];
学科分类号:
070303 ;
081704 ;
摘要:
The construction of the fragments C-1-C-9 3 and C-17-C-27 4a of the bryostatins in a enantioselective and highly diastereoselective fashion is described. The usefulness of the ''chiron'' approach is illustrated with the synthesis of these fragments from, respectively, D-pantolactone (6) and D-isobutyl lactate (23) as chiral templates.
机构:
Ecole Super Phys & Chim Ind Ville Paris, CNRS, Chim Organ Lab, F-75231 Paris 05, FranceEcole Super Phys & Chim Ind Ville Paris, CNRS, Chim Organ Lab, F-75231 Paris 05, France
BouzBouz, S
Cossy, J
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h-index: 0
机构:
Ecole Super Phys & Chim Ind Ville Paris, CNRS, Chim Organ Lab, F-75231 Paris 05, FranceEcole Super Phys & Chim Ind Ville Paris, CNRS, Chim Organ Lab, F-75231 Paris 05, France