ACADSTAFF UGM

CREATION
Title : Indole macrocycles formed by diindolylmethane ring closure
Author :

Prof. Drs. Bambang Purwono, M.Sc., Ph.D. (1) Naresh Kumar (2) David StC. Black (3)

Date : 18 2022
Keyword : Diindolylmethanes,Formaldehyde,Indoles,Lactams,Lactones,Macrocycles Diindolylmethanes,Formaldehyde,Indoles,Lactams,Lactones,Macrocycles
Abstract : Indole containing macrocyclic compounds can be formed from suitable diindolyl diesters and diamides by acidcatalysed reaction with formaldehyde to generate a 2,2′-linkage in the ring closure step. The alternative protocol in which macrocyclisation is attempted by lactone or lactam formation from starting 2,2′- diindolylmethane systems was unsuccessful in our examples.
Group of Knowledge : Kimia
Original Language : English
Level : Internasional
Status :
Published
Document
No Title Document Type Action
1 2022-Arkivoc-David Black-2.pdf
Document Type : [PAK] Full Dokumen
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