Conjugate addition of curcumins to chalcones and azodicarboxylates

Ayyagari, Narasimham ; Mehta, Ankit ; Gopi, Elumalai ; Deb, Indubhusan ; Mobin, Shaikh M. ; Namboothiri, Irishi N.N. (2013) Conjugate addition of curcumins to chalcones and azodicarboxylates Tetrahedron, 69 (29). pp. 5973-5980. ISSN 0040-4020

Full text not available from this repository.

Official URL: http://doi.org/10.1016/j.tet.2013.04.083

Related URL: http://dx.doi.org/10.1016/j.tet.2013.04.083

Abstract

Cascade double Michael reaction of curcumins with chalcones in the presence of Cs2CO3 in CH3CN provided highly functionalized cyclohexanones in moderate to good yields (35-77%) and good to excellent diastereoselectivities (81:19 to 95:05). Similar reaction of curcumins with azodicarboxylates in the presence of DMAP in CH3CN stopped at the single Michael addition stage affording novel hydrazinodicarboxylates of curcumins in good to excellent yields (65-85%).

Item Type:Article
Source:Copyright of this article belongs to Elsevier Science.
ID Code:121558
Deposited On:19 Jul 2021 08:53
Last Modified:19 Jul 2021 08:53

Repository Staff Only: item control page