435286-54-7

Upstream product

• 110-87-2 3,4-dihydro-2H-pyran 
• 435286-45-6 (+)-(2S)-5-benzenesulfonyl-2-(tetrahydropyran-2-yloxy)-1-tosyloxy-pent-3-ene 
• 435286-39-8 (-)-(2S)-5-benzenesulfonyl-1-tosyloxy-pent-3-ene-2-ol 
• 435286-42-3 (-)-(2S)-5-benzenesulfonyl-1-iodo-pent-3-ene-2-ol 
• 435286-36-5 (-)-(2S)-5-benzenesulfonyl-pent-3-ene-1,2-diol 
• 219926-63-3 (+)-(4S)-2,2-Dimethyl-4-[(E)-3-phenylsulfonylprop-1-enyl]-1,3-dioxolane 
• 613682-71-6 (+)-(2S,3Z)-5-benzenesulfonyl-1-tosyloxy-pent-3-en-2-ol 
• 613682-72-7 (+)-(2S,3Z)-5-benzenesulfonyl-1-iodo-pent-3-en-2-ol 
• 613682-70-5 (+)-(2S,3Z)-5-benzenesulfonyl-pent-3-ene-1,2-diol 
• 219926-64-4 (-)-(4S)-2,2-Dimethyl-4-[(Z)-3-phenylsulfonylprop-1-enyl]-1,3-dioxolane 
• 613682-73-8 (-)-(2S,3Z)-5-benzenesulfonyl-1-iodo-2-(tetrahydropyran-2-yloxy)-pent-3-ene 
• 435286-48-9 (+)-(2S)-5-benzenesulfonyl-1-iodo-2-(tetrahydropyran-2-yloxy)-pent-3-ene 

Downstream Products

• 435286-65-0 (-)-(1R,2R)-2-(2-benzenesulfonylethyl)-1-(tetrahydropyran-2-yloxy)-cyclopropane 

Relevant academic research and scientific papers

Enantiomerically pure cis- and trans-2-substituted cyclopropanols from allylic sulfones

Enantiomerically pure cis- and trans-2-substituted cyclopropanols have been obtained from allylic sulfones derived from (R)-glyceraldehyde, in good yields.

Stereocontrolled synthesis of cyclopropanol amino acids from allylic sulfones: Conformationally restricted building blocks

(Matrix presented) A new amino acid methyl ester with a cyclopropanol has been synthesized starting from the allyl sulfone 10. The starting material, 10, could be obtained in both enantiomeric forms. The stereoselectivity of the cyclopropane formation has

Diastereoselective synthesis of enantiomerically pure 1,2-disubstituted cyclopropanols from allylic sulfones

Enantiomerically pure 1,2-disubstituted cyclopropanols have been obtained from allylic sulfones derived from (R)-glyceraldehyde, in good yield.