Wada,K.; Ishida,T., Journal of the Chemical Society. Perkin transactions I, 1979, p. 1154 - 1158
摘要:
DOI:
作为产物:
描述:
6-((E)-(R)-6-Hydroxy-hept-1-enyl)-2,2-dimethyl-[1,3]dioxin-4-one 以
甲苯 为溶剂,
反应 4.0h,
以68%的产率得到(+)-Diplodiaalide A
参考文献:
名称:
A new, highly efficient, selective methodology for formation of medium-ring and macrocyclic lactones via intramolecular ketene trapping: an application to a convergent synthesis of (-)-kromycin
An efficient stereoselective total synthesis of Diplodialide A has been achieved from inexpensive and commercially available starting material (R)-propylene oxide. This linear synthesis utilizes Wittig reaction, alkylation of 1,3-dithiane and Yamaguchi macrolactonization as key steps.
Diplodialide A 的高效立体选择性全合成已由廉价且可商购的起始材料 (R)-环氧丙烷实现。这种线性合成利用 Wittig 反应、1,3-二噻烷的烷基化和 Yamaguchi 大环内酯化作为关键步骤。
BOECKMAN, ROBERT K. (JR);PRUITT, JAMES R., J. AMER. CHEM. SOC., 111,(1989) N1, C. 8286-8288
作者:BOECKMAN, ROBERT K. (JR)、PRUITT, JAMES R.
DOI:——
日期:——
A new, highly efficient, selective methodology for formation of medium-ring and macrocyclic lactones via intramolecular ketene trapping: an application to a convergent synthesis of (-)-kromycin
作者:Robert K. Boeckman、James R. Pruitt
DOI:10.1021/ja00203a044
日期:1989.10
Wada,K.; Ishida,T., Journal of the Chemical Society. Perkin transactions I, 1979, p. 1154 - 1158