22118-00-9Relevant articles and documents
Regio- and stereoselective rearrangement reactions of various α,β- epoxy acylates: Suitable combination of acyl groups and Lewis acids
Kita, Yasuyuki,Yoshida, Yutaka,Kitagaki, Shinji,Mihara, Sachiko,Fang, Dai-Fei,Furukawa, Akihiro,Higuchi, Kazuhiro,Fujioka, Hiromichi
, p. 4979 - 4998 (1999)
Regio- and stereoselective rearrangement reactions of various α,β- epoxy acylates including acyclic, monocyclic and bicyclic systems occurred under a suitable combination of acyl groups (benzoyl, p-nitrobenzoyl, camphanoyl) and Lewis acids (BF3
Acid-promoted rearrangement of α,β-epoxy acylates: Remarkable effects of an acyl group and a Lewis acid
Kita, Yasuyuki,Kitagaki, Shinji,Yoshida, Yutaka,Mihara, Sachiko,Fang, Dai-Fei,Fujioka, Hiromichi
, p. 1061 - 1064 (2007/10/03)
Remarkable steric and electrostatic effects of acyl groups and exceptionally bulky Lewis acid, (MABR), which make the rearrangement reaction applicable to various types of reaction systems including acyclic ones in the acid-promoted rearrangement of α,β-epoxy acylates, were found.