Towards the Total Synthesis of Ambruticin: Preparation of the Fully Functionalised Right-Hand Portion Using the Intramolecular Silyl-Modified Sakurai (ISMS) Annulation
The Intramolecular Silyl-Modified Sakurai (ISMS) reaction. Synthetic studies towards ambruticine
作者:István E Markó、Daniel J Bayston
DOI:10.1016/s0040-4020(01)85240-6
日期:1994.1
The ISMS reaction has been used to efficiently construct the right-hand portion 3 of the antifungal antibiotic ambruticine 1.
ISMS反应已用于有效构建抗真菌抗生素氨苄青霉素1的右侧部分3。
Towards the Total Synthesis of Ambruticin: Preparation of the Fully Functionalised Right-Hand Portion Using the Intramolecular Silyl-Modified Sakurai (ISMS) Annulation
作者:István E. Markó、Daniel J. Bayston
DOI:10.1055/s-1996-4185
日期:1996.2
The concise synthesis of the fully functionalised right-hand dihydropyran subunit of the antifungal antibiotic ambruticin (1), using the ISMS annulation as the key-step, is described.