1586768-67-3Relevant academic research and scientific papers
Synthesis of Cyclopropanoids via Substrate-Based Cyclization Pathways
Mishra, Uttam K.,Patel, Kaushalendra,Ramasastry
, p. 175 - 179 (2019)
A series of unexpected reactions triggered by the dimethyloxosulfonium methylide led to the discovery of unconventional approaches for the synthesis of cyclopropa-fused tetralones and indeno-spirocyclopropanes. These highly functionalized structures were further elaborated in one step to privileged scaffolds such as tetralones, indenones, and fluorenones. As a whole, the results presented herein establish new diversity-oriented folding pathways.
NHC-catalyzed oxidative cyclization reaction for the synthesis of 3-substituted phthalides
Youn, So Won,Song, Hyoung Sub,Park, Jong Hyub
supporting information, p. 2388 - 2393 (2014/04/03)
An efficient NHC-catalyzed domino oxidation/oxa-Michael addition reaction of 2-alkenylbenzaldehydes has been developed to afford 3-substituted phthalides bearing a C3-stereogenic center with a broad substrate scope and wide functional group tolerance. The preliminary results of the asymmetric process have been provided as well. the Partner Organisations 2014.
