期刊
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 130, 期 12, 页码 3740-+出版社
AMER CHEMICAL SOC
DOI: 10.1021/ja800001h
关键词
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Propargylic pivalates with electronically unbiased internal alkynes are selectively transformed into (1Z,3E)-2-pivaloxy-1,3-dienes containing various functionalities. The unusual selectivity of 1,2-acyloxy migration over the structurally preferred 3,3-rearrangement is realized. This reaction is highly stereoselective and offers rapid access to dienes for one-pot intra-/intermolecular Diels-Alder reactions either under thermal conditions or with Lewis acid catalysis.
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