Cobalt(II) Phthalocyanine‐Catalyzed Highly Chemoselective Reductive Amination of Carbonyl Compounds in a Green Solvent | Zendy

Kumar Vishal | Zendy; Sharma Upendra | Zendy; Verma Praveen K. | Zendy; Kumar Neeraj | Zendy; Singh Bikram | Zendy

AI Assistant Blog Pricing

Home ZAIA Blog

Premium

Cobalt(II) Phthalocyanine‐Catalyzed Highly Chemoselective Reductive Amination of Carbonyl Compounds in a Green Solvent

Author(s) -

Kumar Vishal,

Sharma Upendra,

Verma Praveen K.,

Kumar Neeraj,

Singh Bikram

Publication year - 2012

Publication title -

advanced synthesis and catalysis

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 1.541

H-Index - 155

eISSN - 1615-4169

pISSN - 1615-4150

DOI - 10.1002/adsc.201100645

Subject(s) - chemistry , reductive amination , alkene , cobalt , nitrile , amide , catalysis , organic chemistry , solvent , amination , chemoselectivity , nitro , acetonitrile , alkyl

Cobalt phthalocyanine has been employed for the highly chemoselective reductive amination of aldehydes and ketones in ethanol as a green solvent. A large range of functional groups such as nitro, acid, amide, ester, nitrile, halogen, lactone, methoxy, hydroxy, alkene, N ‐benzyl, O ‐benzyl and heterocyclic rings were well tolerated under the present reaction conditions.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here

Accelerating Research