10.1021/acs.orglett.5b02403.s004
David
A. Petrone
David
A.
Petrone
Andy Yen
Andy
Yen
Nicolas Zeidan
Nicolas
Zeidan
Mark Lautens
Mark
Lautens
Dearomative Indole Bisfunctionalization via a Diastereoselective
Palladium-Catalyzed Arylcyanation
American Chemical Society
2015
cyanation mechanism
diastereoselectivity
Pd
bisfunctionalization
diastereoselective arylcyanation
indole
Dearomative Indole Bisfunctionalization
ArylcyanationThe
method
stereocenter
dearomative
formation
benzylic
Diastereoselective
indoline scaffolds
2015-10-02 00:00:00
Dataset
https://acs.figshare.com/articles/dataset/Dearomative_Indole_Bisfunctionalization_via_a_Diastereoselective_Palladium_Catalyzed_Arylcyanation/2126452
The first Pd-catalyzed
dearomative indole bisfunctionalization
via a diastereoselective arylcyanation is reported. This method facilitates
the formation of diverse indoline scaffolds bearing congested stereocenters
with high levels of diastereoselectivity. This also represents the
first example of a cyanation mechanism involving a 2° benzylic
Pd(II) intermediate.