All articles of this category Key steps in a stereoselective synthesis of Herboxidiene A, a diastereoisomer of the natural herbicide Herboxidiene, include a Hoppe homoaldol reaction, a copper(I)-mediated 1,2-metallate rearrangement, and a one-pot synthesis of a diene fragment from condensation of a lithiated benzothiazolyl sulfone and an aldehyde. herbicide - 1,2-metallate rearrangement - organocuprate - homoaldol reaction - Julia olefination - directed epoxidation
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Smith et al. (1996) studied this question.
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