28098-84-2Relevant articles and documents
Nickel-Catalyzed Favorskii-Type Rearrangement of Cyclobutanone Oxime Esters to Cyclopropanecarbonitriles
Fang, Ping,Mei, Tian-Sheng,Shuai, Bin
supporting information, p. 1637 - 1641 (2021/10/02)
A nickel-catalyzed base-promoted rearrangement of cyclobutanone oxime esters to cyclopropanecarbonitriles was developed. The ring opening of cyclobutanone oxime esters occurs at the sterically less hindered side. A base-promoted nickelacyclobutane intermediate, formed in situ, is assumed to be involved in the formation of the product.
Towards nitrile-substituted cyclopropanes-a slow-release protocol for safe and scalable applications of diazo acetonitrile
Hock, Katharina J.,Spitzner, Robin,Koenigs, Rene M.
supporting information, p. 2118 - 2122 (2017/07/24)
Diazo acetonitrile has long been neglected despite its high value in organic synthesis due to a high risk of explosions. Herein, we report our efforts towards the transient and safe generation of this diazo compound, its applications in iron catalyzed cyclopropanation and cyclopropenation reactions and the gram-scale synthesis of cyclopropyl nitriles.
Incremental solvation precedes ion-pair separation in enantiomerization of a cyano-stabilized Grignard reagent
Patwardhan, Neeraj N.,Gao, Ming,Carlier, Paul R.
supporting information; experimental part, p. 12250 - 12253 (2011/12/15)
Concerted or stepwise? Ion-pair separation is often proposed as a mechanism for enantiomerization of organolithium reagents in ethereal solvents. But what is the timing of the solvation and bond-cleavage events? Are they concerted, or does one precede the
