107942-03-0Relevant articles and documents
Chiron approach towards the synthesis of (2S,3R)-3-hydroxyornithine, (2S,3R)-3-hydroxylysine and tetrahydroazepine core of (?)-balanol
Rohokale, Rajendra,Dhavale, Dilip
, p. 4550 - 4555 (2016)
D-Glucose derived synthon 4 was successfully utilized for the synthesis of (2S,3R)-β-hydroxyornithine 1, (2S,3R)-β-hydroxylysine 2 and tetrahydroazepine core of balanol 3.
Stereochemical Correlation of Proclavamimic Acid and Syntheses of erythro- and threo-L-β-Hydroxyornithine from an Improved Vinylglycine Synthone
Krol, Walter J.,Mao, Shin-shan,Steele, Diana L.,Townsend, Craig A.
, p. 728 - 731 (2007/10/02)
The Hanessian method to prepare the N-Cbz-L-vinylglycine methyl ester has been improved to obtain reproducibility an alternately protected version of this useful synthon in optically pure, crystalline form.A nitrone cycloaddition route has been developed
A 1,3-Dipolar Cycloaddition Route to the 3(R)- and 3(S)-Hydroxy-(2S)-arginines
Wityak, John,Gould, Steven J.,Hein, Scott J.,Keszler, Douglas A.
, p. 2179 - 2183 (2007/10/02)
The 3(R)- and 3(S)-hydroxy-(2S)-arginines (4a and 4b) were prepared from the corresponding β-hydroxyornithines (3a and 3b) via methyl 2(S)-acetates (5a and 5b).The isoxazolidines 5 were prepar
