1045346-01-7

Upstream product

• 1045346-00-6 (+)-(2S,3S,R_S)-2-phenyl-3-(p-tolylsulfinyl)-3,6-dihydro-2H-pyran 
• 729593-99-1 (-)-(2S,3R,R_S)-2-phenyl-3-(p-tolylsulfinyl)-3,6-dihydro-2H-pyran 
• 729593-95-7 (-)-(S)-2-(Z)-4-(Z)-5-phenyl-4-(p-tolylsulfinyl)penta-2,4-dien-1-ol 
• 591-51-5 phenyllithium 
• 496-62-8 D-xylal 

Downstream Products

• 1082073-91-3 phenyl 4-O-acetyl-2,3-dideoxy-α-L-erythro-pent-2-enopyranoside 

Relevant academic research and scientific papers

Regio- and stereoselective behavior of l-arabinal-derived vinyl epoxide in nucleophilic addition reactions. Comparison with conformationally restricted d-galactal-derived analogs

Abstract The regio- and stereoselectivity of the addition reactions of O-, C-, N-, and S-nucleophiles to l-arabinal-derived vinyl epoxide 2, the simplest non-conformationally restricted glycal-derived vinyl epoxide, has been examined and compared with the

[2,3]-Sigmatropic rearrangements of 3-sulfinyl dihydropyrans: application to the syntheses of the cores of ent-dysiherbaine and deoxymalayamicin A

(Chemical Equation Presented) The [2,3]-sigmatropic rearrangement of a variety of configurationally stable diastereomeric allylic sulfinyl dihydropyrans, produced by base-promoted cyclization of sulfinyl dienols, has been studied. In some cases, the effic