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标题：Highly Enantioselective Addition of Phenylacetylene to Aldehydes Catalyzed by a Camphorsulfonamide Ligand
来源：《有机快报》2004年6卷8期1193-1195页
作者：兰州大学生命科学学院生物化学与分子生物学系 Zhao-Qing Xu（许兆青）, Chao Chen（陈超）, Jiang-Ke Xu（许江珂）, Ming-Bo Miao, Wen-Jin Yan（闫文锦）
兰州大学生命科学学院生物化学与分子生物学系、北京大学化学院 教育部生物有机化学与分子工程重点实验室 Rui Wang（王锐）
Research Fronts: HIGHLY ENANTIOSELECTIVE PHENYLACETYLENE ADDITION; HIGHLY ENANTIOSELECTIVE ADDITION; ENANTIOSELECTIVE ADDITIONS; AROMATIC KETONES CATALYZED; ALDEHYDES CATALYZED
领域：化学
摘要：The asymmetric addition of phenylacetylene to aldehydes was carried out by using a camphorsulfonamide titanium complex as a catalyst. The reactions proceeded under mild conditions and gave the products with good yields and high ees. This system is very useful for the synthesis of chiral propargylic alcohol.
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