131233-29-9

Upstream product

• 109-80-8 1.3-propanedithiol 
• 131142-87-5 (R)-2-[(2S,4S,5R)-4-Methyl-5-phenyl-3-(toluene-4-sulfonyl)-oxazolidin-2-yl]-propan-1-ol 
• 131142-86-4 (R)-2-[(2R,4S,5R)-4-Methyl-5-phenyl-3-(toluene-4-sulfonyl)-oxazolidin-2-yl]-propan-1-ol 

Downstream Products

• 186448-73-7 Toluene-4-sulfonic acid (R)-2-[1,3]dithian-2-yl-propyl ester 
• 131142-71-7 (S)-3,3,3-Trifluoro-2-methoxy-2-phenyl-propionic acid (R)-2-[1,3]dithian-2-yl-propyl ester 
• 930803-40-0 C₅₉H₁₀₂O₉S₂Si₂ 
• 930803-38-6 C₅₉H₁₀₂O₉S₂Si₂ 
• 930803-37-5 C₄₁H₆₆O₆S₂Si 
• 930803-73-9 C₃₅H₅₂O₆S₂ 
• 930803-36-4 C₃₅H₅₀O₆S₂ 
• 930803-35-3 C₄₁H₆₆O₆S₂Si 
• 930803-55-7 C₃₅H₅₂O₆S₂ 
• 1301605-24-2 C₂₁H₃₀O₄S₂ 
• 1301605-23-1 C₂₁H₃₀O₄S₂ 

Relevant academic research and scientific papers

STEREOCONVERGENT CROTYLSTANNANE ADDITION TO NOR-EPHEDRINE-DERIVED 2-METHOXY OXAZOLIDINES. A CLUE TOWARDS A SYNCLINAL TRANSITION STATE GEOMETRY

The Lewis acid promoted addition of crotyl-n-tributylstannane to a nor-ephedrine-derived 2-methoxy-oxazolidine has been studied.This stereoconvergent reaction allows highly selective C-C bond formation and takes place with opposite stereochemistry with respect to the analogous silylketenethioacetal addition.This result suggests a preference for a synclinal transition state geometry.