35334-80-6

Upstream product

• 38270-72-3 dimethyl 2,3-O-benzylidene-L-tartrate 
• 35572-34-0 (4S,5S)-4,5-dihydroxymethyl-2-phenyldioxolane 

Downstream Products

• 101514-21-0 1-cyano-1-thiophenyl-3,4-dibenzyloxycyclopentane 
• 118653-94-4 Toluene-4-sulfonic acid (S)-2-benzyloxy-2-(S)-oxiranyl-ethyl ester 
• 101514-20-9 (3S,4S)-3-Benzyloxy-4-hydroxy-1-phenylsulfanyl-cyclopentanecarbonitrile 
• 101514-13-0 (2R,3R)-3-Benzyloxy-1,4-dibromo-butan-2-ol 
• 101514-19-6 (S)-2-(1-Benzyloxy-vinyl)-oxirane 
• 101514-16-3 (S)-2-((R)-1-Benzyloxy-2-bromo-ethyl)-oxirane 
• 908260-83-3 C₂₅H₂₈O₈S₂ 
• 101514-10-7 (4R,5R)-4,5-bis(bromomethyl)-2-phenyl-1,3-dioxolane 
• 69087-52-1 (2S,3S)-4,5-dimethyl-2-phenyl-1,3-dioxolane 

Relevant academic research and scientific papers

NOVEL (4+1) FRAGMENT COMBINATION APPROACH TO CHIRAL CYCLOPENTANOIDS FROM TARTARIC ACID

A chiral cyclopentanoid building block 29 has been synthesized in a "one pot" cyclization process from epoxides 22-25 (which are readily accessible from (R,R)-(+)-tartaric acid) with the carbanion derived from phenylthioacetonitrile (PhS-CH2-CN).