121824-05-3

Upstream product

• 104891-35-2 (R) 3-chloro 1-p-tolylsulfinyl 2-propanone 
• 1519-39-7 (R)-methyl p-tolyl sulfoxide 
• 121824-03-1 (2S)-1-chloro-3-<(R)-(4-methylphenyl)sulphinyl>-2-propanol 

Downstream Products

• 121824-08-6 <2(R),4(Z),S(R)> 1-p-tolylsulfinyl 4-decen-2-ol 
• 121824-07-5 (E)-(R)-1-((R)-Toluene-4-sulfinyl)-dec-4-en-2-ol 
• 136580-80-8 <2(S),4(Z),S(R)> 1-p-tolylsulfinyl 4-decen-2-ol 
• 136580-81-9 <2(R),4(Z),S(R)> 2-t-butyldimethylsilyloxy 1-p-tolylsulfinyl 4-decene 
• 136580-79-5 Acetic acid (Z)-(R)-2-(tert-butyl-dimethyl-silanyloxy)-1-p-tolylsulfanyl-dec-4-enyl ester 
• 155570-01-7 <2(R),4(E),S(R)>-8-chloro-1-(p-tolylsulfinyl)-4-octene-2-ol 

Relevant academic research and scientific papers

OPTICALLY ACTIVE α-SULFINYL EPOXIDES: PRECURSORS OF CHIRAL FUNCTIONALIZED HOMOALLYLIC ALCOHOLS

An asymmetric synthesis of chiral functionalized homoallylic alcohols in both configurations is described from the corresponding optically active α-sulfinyl epoxides.

Asymmetric Synthesis of the C-1-C-8 Fragment of Leukotriene B4 and C-11-C-20 Fragments of Leukotriene B4 and 12(S)-Hydroxy-5,8,14(Z), 10(E) Eicosatetraenoic Acid

An asymmetric synthesis of the C-1-C-8 fragment of LTB4 based on the reduction of optically active β-ketosulfoxides is described as well as the asymmetric synthesis of the C-11-C-20 fragments of LTB4 and 12(S)-hydroxy-5,8,14(Z), 10(E