In:
Advanced Synthesis & Catalysis, Wiley, Vol. 360, No. 3 ( 2018-02), p. 401-405
Kurzfassung:
Axial naphthols are applied in asymmetric halogenative dearomatization reactions under simple and mild conditions in the work presented herein. The axial‐to‐central chirality conversion is efficiently accomplished, and the desired halogenated dearomatization products are obtained in high yields and enantioselectivities. By using commercially available halogenation reagents, the asymmetric fluorinative, chlorinative and brominative dearomatization reactions of axial naphthols derived from BINOLs are achieved. (BINOL=1,1′‐Bi‐2‐naphthol) magnified image
Materialart:
Online-Ressource
ISSN:
1615-4150
,
1615-4169
DOI:
10.1002/adsc.201700745
Sprache:
Englisch
Verlag:
Wiley
Publikationsdatum:
2018
ZDB Id:
2041384-1
ZDB Id:
2033084-4