epi-Chrysotricine 6 was synthesized by a cascade stereoselective oxidative cyclization of 5-hydroxyalkene 3 using tert-butyl hydroperoxide(TBHP) catalyzed by VO(acac)2.
A practical and cheap method for synthesis of C-4 carboxylic acid substituted kainic acid analogue 5 and its epimer 6 from trans-4-hydroxyproline is described. Using this method, more interesting intermediates and ana...A practical and cheap method for synthesis of C-4 carboxylic acid substituted kainic acid analogue 5 and its epimer 6 from trans-4-hydroxyproline is described. Using this method, more interesting intermediates and analogues could be obtained easily.展开更多
(±)Chrysotricine 1 was synthesized by a facile route. The key steps in the synthesis were aldol condensation of dilithium salt of harman 4 with 6 -methyl-5-hepten-2-one 5 and cyclization of compound 6 using MCPBA...(±)Chrysotricine 1 was synthesized by a facile route. The key steps in the synthesis were aldol condensation of dilithium salt of harman 4 with 6 -methyl-5-hepten-2-one 5 and cyclization of compound 6 using MCPBA. The 1HNMR specmim of synthetic product was identical to that of the natural sample.展开更多
基金the National Research Center for Analysis of Drugs and Metabolites for recording NMR and MS data. This project was partially fo
文摘epi-Chrysotricine 6 was synthesized by a cascade stereoselective oxidative cyclization of 5-hydroxyalkene 3 using tert-butyl hydroperoxide(TBHP) catalyzed by VO(acac)2.
文摘A practical and cheap method for synthesis of C-4 carboxylic acid substituted kainic acid analogue 5 and its epimer 6 from trans-4-hydroxyproline is described. Using this method, more interesting intermediates and analogues could be obtained easily.
文摘(±)Chrysotricine 1 was synthesized by a facile route. The key steps in the synthesis were aldol condensation of dilithium salt of harman 4 with 6 -methyl-5-hepten-2-one 5 and cyclization of compound 6 using MCPBA. The 1HNMR specmim of synthetic product was identical to that of the natural sample.
