The Journal of Organic Chemistry

An effective strategy for acyclic synthesis via iterative rearrangement of allylic glycolates. Synthesis of a pine sawfly pheromone

J Kallmerten, M Balestra

文献索引：Kallmerten, James; Balestra, Michael Journal of Organic Chemistry, 1986 , vol. 51, # 14 p. 2855 - 2857

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被引用次数: 23

摘要

Summary: The stereocontrolled preparation of extended acyclic systems using the iterative enolate Claisen rear- rangement of allylic glycolates is described. This strategy has been demonstrated in the stereospecific synthesis of a pine sawfly pheromone. ... Sir: The development of stereoselective techniques for use in the linear elaboration of complex acyclic targets has been a focus of considerable attention in recent years.'+ While linear construction of extended acyclic systems offers ...