Ontology highlight
ABSTRACT:
SUBMITTER: Yin Q
PROVIDER: S-EPMC5707459 | biostudies-other | 2015 Jul
REPOSITORIES: biostudies-other
Yin Qin Q Wang Shou-Guo SG Liang Xiao-Wei XW Gao De-Wei DW Zheng Jun J You Shu-Li SL
Chemical science 20150427 7
An organocatalytic asymmetric chlorinative dearomatization of naphthols was realized for the first time, providing chiral naphthalenones with a Cl-containing all-substituted stereocenter in excellent yields and enantioselectivity (up to 97% yield and 96% ee). The reaction features mild reaction conditions, good tolerance of diverse functional groups and simple reaction operation. ...[more]