878476-05-2Relevant academic research and scientific papers
Synthesis and Formation Mechanism of a Compound with an Unprecedented Skeleton: Dodecahydro-4,10:5,9-diepoxydipyrrolo[3,4-b:3′,4′-f][1,5]diazocine
Shinoda, Misaki,Morita, Nobuyoshi,Tanaka, Kosaku,Hashimoto, Yoshimitsu,Ban, Shintaro,Tamura, Osamu
, p. 1238 - 1243 (2020/12/18)
The reaction of N-(2-{[(tert-butyldimethylsilyl)oxy]imino}ethyl)-4-methyl-N-(3-phenylprop-2-yn-1-yl)benzenesulfonamide (6b) with BF3·OEt2 afforded a compound with an unprecedented dodeca-hydro-4,10:5,9-diepoxydipyrrolo[3,4-b:3′,4′-f]
Triflic Acid-Catalyzed Enynes Cyclization: A New Strategy beyond Electrophilic π-Activation
Yu, Zhunzhun,Liu, Lu,Zhang, Junliang
supporting information, p. 8488 - 8492 (2016/07/11)
The cyclization of enynes, catalyzed by a transition metal, represents a powerful tool to construct an array of cyclic compounds through electrophilic π-activation. In this paper, we disclose a new and efficient strategy for enynes cyclization catalyzed b
Palladium(0)-catalyzed alkylative cyclization of alkynals and alkynones: Remarkable trans-addition of organoboronic reagents
Tsukamoto, Hirokazu,Ueno, Tatsuhiko,Kondo, Yoshinori
, p. 1406 - 1407 (2007/10/03)
Palladium/monophosphine complexes catalyze trans-selective arylative, alkenylative, and alkylative cyclization reactions of alkynals and alkynones with organoboronic reagents. These reactions afford six-membered allylic alcohols with endo-tri- or tetrasub
