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  • Highly enantioselective phenylacetylene additions to ketones catalyzed by (S)-BINOL-Ti complex.

Highly enantioselective phenylacetylene additions to ketones catalyzed by (S)-BINOL-Ti complex.

Organic letters (2004-11-05)
Yifeng Zhou, Rui Wang, Zhaoqing Xu, Wenjin Yan, Lei Liu, Yongfeng Kang, Zhijian Han
ABSTRACT

The readily available and inexpensive (S)-BINOL ligand in combination with Ti(O(i)Pr)(4) is an effective chiral catalyst for the catalytic asymmetric addition of alkynylzinc to unactivated simple ketones. Good to excellent enantioselectivities were achieved. No previous case has been reported successfully using BINOL to catalyze the addition of phenylacetylene to unactivated ketones, and thus the utility of BINOL in asymmetric catalysis is expanded.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
1,1′-Bi-2-naphthol, 99%