136580-80-8

Upstream product

• 121824-02-0 (2(R),S(R)) 3-chloro 1-p-tolylsulfinyl 2-propanol 
• 104891-35-2 (R) 3-chloro 1-p-tolylsulfinyl 2-propanone 
• 121824-03-1 (2S)-1-chloro-3-<(R)-(4-methylphenyl)sulphinyl>-2-propanol 
• 1519-39-7 (R)-methyl p-tolyl sulfoxide 
• 121824-05-3 (+)-<2(R),S(R)>-p-tolylsulfinyl-2-methyloxirane 
• 63318-29-6 (Z)-1-iodohept-1-ene 
• 121824-04-2 (+)-<2(S),S(R)>-p-tolylsulfinyl-2-methyloxirane 

Relevant academic research and scientific papers

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

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.