期刊
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 136, 期 23, 页码 8209-8212出版社
AMER CHEMICAL SOC
DOI: 10.1021/ja504374j
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资金
- NIH NIGMS [GM080266]
- Uehara Memorial Foundation
Angularly substituted trans-fused hydroindanes are now accessible by the direct and convergent union of trimethylsilyl (TMS)-alkynes with 4-hydroxy-1,6-enynes by a process that forges three C C bonds, one C H bond, and two new stereocenters. The annulation is proposed to proceed by initial formation of a Ti-alkyne complex (with a TMS-alkyne) followed by regioselective alkcodde-directed coupling with the enyne, stereoselective intramolecular cycloaddition, elimination of phenoxide, 1,3-metallotropic shift, and stereoselective protonation of the penultimate allylic organometallic intermediate. Several examples are given to demonstrate the compatibility of this reaction with substrates bearing aromatic and aliphatic substituents, and an empirical model is presented to accompany the stereochemical observations.
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