引用本文:
Xue Qiang LI, Xue Zhi ZHAO, Pei Nian LIU, Yong Qiang TU. Efficient Synthesis of the C1-C7 Fragment of Didemnaketal A[J]. Chinese Chemical Letters,
2004, 15(7): 757-758.
Citation: Xue Qiang LI, Xue Zhi ZHAO, Pei Nian LIU, Yong Qiang TU. Efficient Synthesis of the C1-C7 Fragment of Didemnaketal A[J]. Chinese Chemical Letters, 2004, 15(7): 757-758.
Citation: Xue Qiang LI, Xue Zhi ZHAO, Pei Nian LIU, Yong Qiang TU. Efficient Synthesis of the C1-C7 Fragment of Didemnaketal A[J]. Chinese Chemical Letters, 2004, 15(7): 757-758.
Efficient Synthesis of the C1-C7 Fragment of Didemnaketal A
摘要:
The stereoselective synthesis of the C1-C7fragment (3R,4S,6R)-3,4-di[(tert-butyl-dimethylsilyl)oxy]-7-hydroxy-6-methylheptan-2-one, which is the crucial intermediate for synthesis of the HIV-1 protease inhibitive didemnaketals, was developed via 12 steps from the natural (+)-pulegone.
English
Efficient Synthesis of the C1-C7 Fragment of Didemnaketal A
Abstract:
The stereoselective synthesis of the C1-C7fragment (3R,4S,6R)-3,4-di[(tert-butyl-dimethylsilyl)oxy]-7-hydroxy-6-methylheptan-2-one, which is the crucial intermediate for synthesis of the HIV-1 protease inhibitive didemnaketals, was developed via 12 steps from the natural (+)-pulegone.
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