TY - JOUR
T1 - Nickel-Catalyzed Phosphine Free Direct N-Alkylation of Amides with Alcohols
AU - Das, Jagadish
AU - Banerjee, Debasis
N1 - Publisher Copyright:
© 2018 American Chemical Society.
PY - 2018/3/16
Y1 - 2018/3/16
N2 - Herein, we developed an operational simple, practical, and selective Ni-catalyzed synthesis of secondary amides. Application of renewable alcohols, earth-abundant and nonprecious nickel catalyst facilitates the transformations, releasing water as byproduct. The catalytic system is tolerant to a variety of functional groups including nitrile, allylic ether, and alkene and could be extended to the synthesis of bis-amide, antiemetic drug Tigan, and dopamine D2 receptor antagonist Itopride. Preliminary mechanistic studies revealed the participation of a benzylic C-H bond in the rate-determining step.
AB - Herein, we developed an operational simple, practical, and selective Ni-catalyzed synthesis of secondary amides. Application of renewable alcohols, earth-abundant and nonprecious nickel catalyst facilitates the transformations, releasing water as byproduct. The catalytic system is tolerant to a variety of functional groups including nitrile, allylic ether, and alkene and could be extended to the synthesis of bis-amide, antiemetic drug Tigan, and dopamine D2 receptor antagonist Itopride. Preliminary mechanistic studies revealed the participation of a benzylic C-H bond in the rate-determining step.
UR - http://www.scopus.com/inward/record.url?scp=85044234299&partnerID=8YFLogxK
U2 - 10.1021/acs.joc.7b03215
DO - 10.1021/acs.joc.7b03215
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C2 - 29441778
AN - SCOPUS:85044234299
SN - 0022-3263
VL - 83
SP - 3378
EP - 3384
JO - Journal of Organic Chemistry
JF - Journal of Organic Chemistry
IS - 6
ER -