87604-60-2Relevant articles and documents
Divergent asymmetric total synthesis of all four pestalotin diastereomers from (R)-glycidol
Moriyama, Mizuki,Nakata, Kohei,Fujiwara, Tetsuya,Tanabe, Yoo
, (2020/01/28)
All four chiral pestalotin diastereomers were synthesized in a straightforward and divergent manner from common (R)-glycidol. Catalytic asymmetric Mukaiyama aldol reactions of readily-available bis(TMSO)diene (Chan’s diene) with (S)-2-benzyloxyhexanal der
TRANSFORMATION OF TARTARIC ACID: A FACILE SYNTHESIS OF DERIVATIVES OF OPTICALLY ACTIVE α-HYDRXYOALDEHYDES
Achmatowicz, Barbara,Wicha, Jerzy
, p. 2999 - 3002 (2007/10/02)
Methods for synthesis of (R)- and (S)-2-benzyloxy- and 2-(t-butyldiphenylsilyloxy)-aldehydes from optically active tartaric acids are described.
ON THE STERIC COURSE OF THE ADDITION OF SOME ORGANOMETALLIC REAGENTS TO (R)-2,3-ISOPROPYLIDENE GLYCERALDEHYDE. SYNTHESIS OF OPTICALLY ACTIVE α-BENZYLOXY ALDEHYDES, ALCOHOLS, CARBOXYLIC ACIDS AND 1,2-DIOLS.
Mulzer, Johann,Angermann, Alfred
, p. 2843 - 2846 (2007/10/02)
Organo-titanium and organo-zinc reagents were added stereoselectively to (R)-2,3-isopropylidene glyceraldehyde (1) to give the alcohols 2/3, which were converted into the optically active derivatives 4-11.