794567-08-1Relevant academic research and scientific papers
Organocatalytic synthesis of (2S,3R)-3-hydroxy-3-methyl-proline (OHMePro), a component of polyoxypeptins, and relatives using OHMePro itself as a catalyst
Yoshitomi, Yayoi,Makino, Kazuishi,Hamada, Yasumasa
, p. 2457 - 2460 (2008/02/05)
An efficient synthesis of (2S,3R)-3-hydroxy-3-methylproline (OHMePro), a component of polyoxypeptins, and relatives was achieved, in which an intramolecular asymmetric aldol reaction of the ketoaldehyde using OHMePro itself as an organocatalyst constitute
Asymmetric synthesis of α-amino 1,3-dithioketals from sulfinimines (N-sulfinyl imines). Synthesis of (2S,3R)-(-)-3-hydroxy-3-methylproline
Davis, Franklin A.,Ramachandar, Tokala,Liu, Hu
, p. 3393 - 3395 (2007/10/03)
(Chemical Equation Presented) N-Sulfinyl α-amino 1,3-dithioketals are prepared in high de and good yield by treating sulfinimines with lithio-1,3-dithianes. Selective removal of the N-sulfinyl or the thioketal groups affords stable α-amino 1,3-dithioketal
A short-step synthesis of (2S,3R)-3-hydroxy-3-methylproline, a component of polyoxypeptins, using a tandem Michael-aldol reaction and optical resolution
Makino, Kazuishi,Suzuki, Tatsuya,Hamada, Yasumasa
, p. 1649 - 1653 (2007/10/03)
A short-step synthesis of (2S,3R)-3-hydroxy-3-methylproline, a component of polyoxypeptins, using a tandem Michael-aldol reaction followed by its optical resolution using (-)-cinchonidine has been achieved.
