336183-01-8Relevant academic research and scientific papers
Chelation-controlled ester-derived titanium enolate aldol reaction: Diastereoselective syn-aldols with mono- and bidentate aldehydes
Ghosh, Arun K,Kim, Jae-Hun
, p. 5621 - 5624 (2007/10/03)
A chelation-controlled and highly diastereoselective synthesis of syn-aldols is described. Aldol reaction of (S)-valinol-derived ester with a variety of aldehydes proceeded with high syn-diastereoselectivities (up to 99:1) and isolated yields (94%).
Ester derived titanium enolate aldol reaction: Chelation controlled diastereoselective synthesis of syn-aldols
Ghosh, Arun K.,Kim, Jae-Hun
, p. 1227 - 1231 (2007/10/03)
A chelation controlled and highly diastereoselective synthesis of syn-aldols is described. Aldol reaction of commercially available L-phenylalaninol derived esters with a variety of bidentate oxyaldehydes proceeded with excellent syn-diastereoselectivities and isolated yields.
Ester derived titanium enolate aldol reaction: Highly diastereoselective synthesis of syn- and anti-aldols
Ghosh, Arun K.,Fidanze, Steve,Onishi, Masanobu,Hussain, Khaja Azhar
, p. 7171 - 7174 (2007/10/03)
Aldol reactions of bidentate aldehydes and cis-1-arylsulfonamido-2-indanyl ester derived titanium enolates proceed with excellent syn-diastereoselectivities and good to excellent isolated yields.
