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Study on the Total Synthesis of 3-Oxo-9β-Acetoxyilicic Acid─The Synthesis of 9β-Acetoxy-3(4),11(13)-Dien-5αH,7αH-12-Eudesmanoic Acid Methyl Ester

Study on the Total Synthesis of 3-Oxo-9β-Acetoxyilicic Acid─The Synthesis of 9β-Acetoxy-3(4),11(13)-Dien-5αH,7αH-12-Eudesmanoic Acid Methyl Ester

作     者:Jiong YANG Zbao Ming XIONG Yong Gang CREN and Yu Lin LI(National Laboratory of Applied Organic Chemistry and Institute of Organic Chemistry,ho University, Lanzhou 730000) 

作者机构:Lanzhou Univ Natl Lab Appl Organ Chem Lanzhou 730000 Peoples R China Lanzhou Univ Inst Organ Chem Lanzhou 730000 Peoples R China 

出 版 物:《Chinese Chemical Letters》 (中国化学快报(英文版))

年 卷 期:1997年第8卷第12期

页      面:0-0页

核心收录:

学科分类:081704[工学-应用化学] 07[理学] 08[工学] 0817[工学-化学工程与技术] 070303[理学-有机化学] 0703[理学-化学] 

主  题:The Synthesis of 9 H,7 H-12-Eudesmanoic Acid Methyl Ester Dien-5 Study on the Total Synthesis of 3-Oxo-9 Acetoxyilicic Acid Acetoxy-3 

摘      要:The synthesis of 99-acetoxy-3(4), 11(13)-dien-5αH 7αH-12-eudesmanoic acid methyl ester (2) was achieved from oxycarvone. The key step is the p-toluenesulfonhydrazide assisted reductiv rearrangement reaction

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