Enantioselective Synthesis of the 1,3‐Dienyl‐5‐Alkyl‐6‐Oxy Motif: Method Development and Total Synthesis
作者:Jie Wang、Chuning Guo、Yaqian Liu、Yunpeng Ji、Hongli Jia、Houhua Li
DOI:10.1002/anie.202400478
日期:2024.4.8
Method development and totalsynthesis have resulted in the enantioselective synthesis of the 1,3-dienyl-5-alkyl-6-oxy motif, and thus expedient total syntheses of three types of natural products (glutarimideantibiotics, α-pyrone polyketides and Lupin alkaloids), completed within 4–7 steps.
Aumann,R. et al., Chemische Berichte, 1979, vol. 112, p. 3644 - 3671
作者:Aumann,R. et al.
DOI:——
日期:——
The stereochemistry of solvolysis of an acyclic allylic epoxide
作者:Neil W. Boaz
DOI:10.1016/0957-4166(94)00339-d
日期:1995.1
In contrast to solvolysis of cyclic allylic epoxides, the acid-catalyzed solvolyses of optically pure 1,2-epoxy-3-butene using water or alcohols show a high degree of inversion stereoselectivity.
The Preparation of 4-Methoxy-2-butenal, a New Dienophile, and Notes on Related Compounds