Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/3763
Title: Diazanorbornene: A Valuable Synthon towards Carbocycles and Heterocycles
Authors: Preethanuj, P
Jijy, E
Prakash, P
Sarngadharan, SC
Vijayan, A
Radhakrishnan, KV
John, J
Keywords: diazanorbornene
metal catalysis
substituted cyclopentanoid
C–H activation
tandem reaction
Issue Date: 15-Nov-2020
Publisher: Wiley
Citation: European Journal of Organic Chemistry;2020(42):6588-6613
Abstract: Desymmetrization of meso compounds is well recognized as a powerful method for delivering biologically relevant molecular skeletons in a few synthetic steps. Heterobicyclic olefins are a class of meso compounds which exhibit exceptional reactivity due to their high ring strain originating from the unfavorable bond angles and eclipsing interactions. Extensive research was carried out towards the synthetic transformations of oxa‐, aza‐, and diazanorbornenes/norbornadienes for the synthesis of a wide variety of carbocycles and heterocycles in a single step, most importantly in a stereo‐ and chemo‐selective manner. This review summarizes the relevant aspects of diazanorbornene reactivity which will inspire the synthetic community for exploiting these highly strained bicyclic systems for the creation of extensive libraries of novel structurally and biologically interesting molecules. The review is divided into several sections based on the type of reactions that diazanorbornenes are subjected to.
URI: https://doi.org/10.1002/ejoc.202001131
http://hdl.handle.net/123456789/3763
Appears in Collections:2020



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