引用本文:
Jiong YANG, Zhao Ming XIONG, Yong Gang CREN, Yu Lin LI. 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[J]. Chinese Chemical Letters,
1997, 8(12): 1041-1042.
Citation: Jiong YANG, Zhao Ming XIONG, Yong Gang CREN, Yu Lin LI. 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[J]. Chinese Chemical Letters, 1997, 8(12): 1041-1042.
Citation: Jiong YANG, Zhao Ming XIONG, Yong Gang CREN, Yu Lin LI. 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[J]. Chinese Chemical Letters, 1997, 8(12): 1041-1042.
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
摘要:
The synthesis of 9β-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 reductive rearrangement reaction.
English
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
Abstract:
The synthesis of 9β-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 reductive rearrangement reaction.
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