78822-87-4

Upstream product

• 78855-50-2 (2R,3R)-4-((R)-Benzenesulfinyl)-3-methyl-butan-2-ol 
• 78855-51-3 C₁₁H₁₅LiO₂S 
• 78822-84-1 1-<2(S)-methyl-3(S)-hydroxy>butylphenyl (R)-sulfoxide 
• 78822-85-2 C₁₁H₁₅LiO₂S 
• 100-68-5 methyl-phenyl-thioether 
• 78822-84-1 (2R,3S)-4-((R)-Benzenesulfinyl)-3-methyl-butan-2-ol 
• 78822-84-1 (2S,3R)-4-((R)-Benzenesulfinyl)-3-methyl-butan-2-ol 
• 78837-34-0 (2S,3R)-3-Methyl-4-phenylsulfanyl-butan-2-ol 
• 100-52-7 benzaldehyde 
• 78822-86-3 (+/-)-(1R^*, 2S^*, 3S^*, 4S^*)-3-methyl-1-phenyl-2-((S^*)-phenylsulfinyl)-1,4-pentanediol 
• 78822-86-3 (+/-)-(1R^*, 2S^*, 3R^*, 4S^*)-3-methyl-1-phenyl-2-((R^*)-phenylsulfinyl)-1,4-pentanediol 
• 78822-86-3 (+/-)-(1S^*, 2R^*, 3S^*, 4S^*)-3-methyl-1-phenyl-2-((R^*)-phenylsulfinyl)-1,4-pentanediol 
• 78822-86-3 (+/-)-(1S^*, 2R^*, 3R^*, 4S^*)-3-methyl-1-phenyl-2-((S^*)-phenylsulfinyl)-1,4-pentanediol 
• 78822-86-3 (+/-)-(1S^*, 2S^*, 3R^*, 4S^*)-3-methyl-1-phenyl-2-((R^*)-phenylsulfinyl)-1,4-pentanediol 

Downstream Products

• 80091-13-0 (2R,3S,4R,5S)-2,3-Dimethyl-5-phenyl-4-phenylsulfanyl-tetrahydro-furan 
• 80091-13-0 (+/-)-(2S^*, 3S^*, 4R^*, 5S^*)-tetrahydro-2,3-dimethyl-5-phenyl-4-(phenylthio)furan 
• 80091-13-0 (+/-)-(2S^*, 3S^*, 4S^*, 5R^*)-tetrahydro-2,3-dimethyl-5-phenyl-4-(phenylthio)furan 
• 80091-13-0 (+/-)-(2S^*, 3R^*, 4R^*, 5S^*)-tetrahydro-2,3-dimethyl-5-phenyl-4-(phenylthio)furan 
• 80091-13-0 (2R,3S,4R,5R)-2,3-Dimethyl-5-phenyl-4-phenylsulfanyl-tetrahydro-furan 
• 80091-13-0 (+/-)-(2S^*, 3R^*, 4S^*, 5S^*)-tetrahydro-2,3-dimethyl-5-phenyl-4-(phenylthio)furan 
• 80091-13-0 (+/-)-(2S^*, 3R^*, 4R^*, 5R^*)-tetrahydro-2,3-dimethyl-5-phenyl-4-(phenylthio)furan 
• 80091-13-0 (2S,3S,4R,5S)-2,3-Dimethyl-5-phenyl-4-phenylsulfanyl-tetrahydro-furan 
• 80091-13-0 (2R,3R,4R,5S)-2,3-Dimethyl-5-phenyl-4-phenylsulfanyl-tetrahydro-furan 
• 80091-13-0 (2S,3S,4R,5R)-2,3-Dimethyl-5-phenyl-4-phenylsulfanyl-tetrahydro-furan 

Relevant academic research and scientific papers

A ROUTE TO STEREOCHEMICALLY COMPLEX TETRAHYDROFURANS USING α-SULFINYL CARBANIONS

Condensation involving α-lithiosulfinyl carbanions provide an efficient strategy for preparation of highly substituted tetrahydrofurans.

STUDIES OF STEREOCHEMICAL CONTROL USING α-LITHIOSULFINYL CARBANIONS

The stereoselectivity in reactions of α-lithiosulfinyl carbanions with aldehydes has been unambiguously established.Steric effects and intramolecular chelation of the associated cation are important factors contributing to the observed outcome.

A Stereoselective Approach to Acyclic Systems via Condensations of α-Lithiosulfinyl Carbanions and Aldehydes

The stereochemical outcome of condensations of α-lithiosulfinyl carbanions with aldehydes is presented, and demonstrates useful methodology for generating 1,2-asymmetry, as well as construction of 1,3-asymmetric relationships in acyclic systems.