10.1021/ol400498a.s001
Yongda Zhang
Yongda
Zhang
Ning Li
Ning
Li
Bo Qu
Bo
Qu
Shengli Ma
Shengli
Ma
Heewon Lee
Heewon
Lee
Nina C. Gonnella
Nina C.
Gonnella
Joe Gao
Joe
Gao
Wenjie Li
Wenjie
Li
Zhulin Tan
Zhulin
Tan
Jonathan T. Reeves
Jonathan T.
Reeves
Jun Wang
Jun
Wang
Jon C. Lorenz
Jon C.
Lorenz
Guisheng Li
Guisheng
Li
Diana C. Reeves
Diana C.
Reeves
Ajith Premasiri
Ajith
Premasiri
Nelu Grinberg
Nelu
Grinberg
Nizar Haddad
Nizar
Haddad
Bruce Z. Lu
Bruce Z.
Lu
Jinhua J. Song
Jinhua J.
Song
Chris H. Senanayake
Chris H.
Senanayake
Asymmetric Methallylation of Ketones Catalyzed by a Highly Active Organocatalyst 3,3′‑F<sub>2</sub>‑BINOL
American Chemical Society
2013
Asymmetric Methallylation
enantioselectivity
loading
Ketones Catalyzed
methallylation
Organocatalyst
mol
ketone
organocatalyst
catalyst
2013-04-05 00:00:00
Journal contribution
https://acs.figshare.com/articles/journal_contribution/Asymmetric_Methallylation_of_Ketones_Catalyzed_by_a_Highly_Active_Organocatalyst_3_3_F_sub_2_sub_BINOL/2427478
(<i>S</i>)-3,3′-F<sub>2</sub>-BINOL has been synthesized for the first time and demonstrated as a highly active organocatalyst for asymmetric methallylation of ketones. Up to 98:2 enantioselectivity and 99% yield were obtained with 5 mol % catalyst loading. The catalyst (<i>S</i>)-3,3′-F<sub>2</sub>-BINOL could be easily recovered and reused.