Enantioselective Synthesis of Core Structures of Hydramicromelins A, B and C

被引:2
作者
Sun, Moran [1 ,2 ]
Dai, Lei [1 ,2 ]
Yang, Hua [1 ,2 ]
Liu, Hongmin [1 ,2 ]
Yu, Dequan [1 ]
机构
[1] Zhengzhou Univ, Sch Pharmaceut Sci, Zhengzhou 450001, Henan, Peoples R China
[2] Collaborat Innovat Ctr New Drug Res & Safety Eval, Zhengzhou 450001, Henan, Peoples R China
基金
中国国家自然科学基金;
关键词
hydramicromelins A; B and C; 2,3]-Meisenheimer rearrangement; chiral tertiary alcohol; epoxidation; ALPHA-KETOESTERS; REARRANGEMENT; DIMETHYLZINC; CONSTRUCTION;
D O I
10.6023/cjoc201802017
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Hydramicromelins A similar to C are coumarin compounds with unique chemical structure and biological activity. With [2,3]-Meisenheimer rearrangemen as a key reaction which has been developed in our laboratory, the core structures of Hydramicromelin A, B and C were synthesized from L-phenylglycine. The route included Wittig reaction, [2,3]-Meisenheimer rearrangement, epoxidation and dihydroxylation reaction, and it was high-yield and high-enantioselectivity.
引用
收藏
页码:2443 / 2449
页数:7
相关论文
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