171358-29-5Relevant academic research and scientific papers
An aza-Payne rearrangement-epoxide ring opening reaction of 2-aziridinemethanols in a one-pot manner: A regio- and stereoselective synthetic route to diastereomerically pure N-protected 1,2-amino alcohols
Ibuka, Toshiro,Nakai, Kazuo,Akaji, Masako,Tamamura, Hirokazu,Fujii, Nobutaka,Yamamoto, Yoshinori
, p. 11739 - 11752 (2007/10/03)
A regio- and stereoselective synthetic route to diastereomerically pure 1,2-amino alcohols via a one-pot aza-Payne rearrangement - epoxide ring opening reaction of 2-aziridinemethanols is reported.
A one-pot aza-Payne rearrangement-epoxide ring opening reaction of 2-aziridinemethanols: A regio- and stereoselective synthetic route to diastereomerically pure 1,2-amino alcohols
Nakai,Nakai, Kazuo,Ibuka,Ibuka, Toshiro,Otaka,Otaka, Akira,Tamamura,Tamamura, Hirokazu,Fujii,Fujii, Nobutaka,Yamamoto,Yamamoto, Yoshinori
, p. 6247 - 6250 (2007/10/02)
A regio- and stereoselective synthetic route to diastereomerically pure 1,2-amino alcohols via a one-pot aza-Payne rearrangement-epoxide ring opening reaction of 2-aziridinemethanols is reported. Satisfactory yields are obtained in excellent diastereoisomeric excesses by successive exposure of 2-aziridinemethanols to potassium hydride and nucleophilic reagents in a one-pot manner.
