Graduate School of Pharmaceutical Sciences, Kumamoto University , 5-1, Oe-honmachi, Chuo-ku, Kumamoto 862-0973, Japan.
Org Lett. 2016 Jan 15;18(2):236-9. doi: 10.1021/acs.orglett.5b03379. Epub 2015 Dec 24.
The enantioselective addition of Grignard reagents to ketones was promoted by a BINOL derivative bearing alkyl chains at the 3,3'-positions. This is the first asymmetric direct aryl Grignard addition to ketones reported to date. A variety of tertiary diaryl alcohols could be obtained in high yields and enantioselectivities without using any other metal source.
手性 3,3'-位带有烷基链的联萘酚衍生物促进了格氏试剂对酮的对映选择性加成。这是迄今为止报道的首例酮的不对称直接芳基格氏加成反应。无需使用任何其他金属源,即可以高产率和对映选择性得到各种叔二芳基醇。