937166-57-9Relevant academic research and scientific papers
Stereoselective strategy for the synthesis of (+)-polyoxamic acid and some polyhydroxylated pyrrolidines
Lingamurthy, Macha,Rajender, Anugula,Rao, Batchu Venkateswara
supporting information, p. 6189 - 6191 (2013/10/22)
An efficient strategy for the synthesis of dihydroxy chiral amino moiety which can be utilized for the synthesis of polyoxamic acid, 1,4-dideoxy-1,4- imino-d-xylitol, and dihydroxy pyrrolidine by using highly diastereoselective nucleophilic addition on ch
4,5-erythro/5,6-threo-Stereoselectivity in vinylogous Mukaiyama aldol addition of a silyloxypyrrole to a threose derivative: stereochemical rationalization and relevance to (+)-castanospermine synthesis
Hunter, Roger,Rees-Jones, Sophie C.M.,Su, Hong
, p. 2819 - 2822 (2007/10/03)
Vinylogous Mukaiyama aldol addition of N-p-methoxybenzyl-4-methoxy-2-trimethylsilyloxypyrrole 7 to bis-MOM threose 6 using SnCl4 as promoter gave the 4,5-erythro/5,6-threo adduct 8, with the correct absolute configurations for the castanospermi
Total synthesis of mycalamide A
Sohn, Jeong-Hun,Waizumi, Nobuaki,Zhong, H. Marion,Rawal, Viresh H.
, p. 7290 - 7291 (2007/10/03)
This communication describes a concise and efficient total synthesis of mycalamide A by the convergent coupling of pederic acid unit with the mycalamine unit. The left-half, (+)-7-benzoylpederic acid, was synthesized from (2R,3R)-3-methylpent-4-en-2-ol in
