83230-73-3Relevant articles and documents
Rh(iii)-Catalyzed intramolecular redox-neutral cyclization of alkenes via C-H activation
Shi, Zhuangzhi,Boultadakis-Arapinis, Melissa,Koester, Dennis C.,Glorius, Frank
, p. 2650 - 2652 (2014/03/21)
Biologically interesting fused oligocyclic lactams have been prepared via an intramolecular redox-neutral cyclization process. By the proper choice of the substrates with a wide variety of tethered olefins, the less favored C-H bond can be activated and f
A synthetic study of dibenzo-aromatic macrolactams
Brown, David P.,Wong, Thomas
experimental part, p. 149 - 161 (2010/06/14)
Efforts to generate benzenoid macrolactams in the development of hybrid molecules as New Chemical Entities are described. The olefin metathesis protocol was adopted in facilitating the cyclization process.
Synthesis of novel aromatic macrolactones via ring closing metathesis of substituted phenylalkanoic acid allylic esters
Brown, David P.,Duong, Hoan Q.
, p. 435 - 443 (2008/09/19)
(Chemical Equation Presented) Stable aromatic macrolactones have been synthesized and characterized from 2- and 3-substituted phenylalkanoic acid systems in modest yields.
