83333-89-5

Upstream product

• 52022-82-9 (E)-5-bromopenta-1,3-diene 
• 2973-86-6 lithium thiophenoxide 
• 5284-13-9 (3E)-2-hydroxy-1-phenylthio-3-pentene 
• 108-98-5 thiophenol 
• 931-59-9 benzenesulfenyl chloride 
• 126690-75-3 ((E)-5-Bromo-pent-2-enylsulfanyl)-benzene 
• 13307-75-0 (phenylthio)methyllithium 

Downstream Products

• 103216-36-0 (2-Methoxy-pent-4-enylsulfanyl)-benzene 
• 84230-76-2 trans-1-Phenylsulfinylmethyl-1,3-butadiene 
• 103216-31-5 C₁₁H₁₁LiS 
• 103229-44-3 (E)-2-Methyl-3-phenylsulfanyl-hepta-4,6-dien-2-ol 
• 137905-44-3 (E)-1-phenylsulphenyl-1-deutero-2,4-pentadiene 
• 84230-81-9 Benzoic acid (2E,4E,6E,9Z)-1-(4-methoxycarbonyl-butyl)-pentadeca-2,4,6,9-tetraenyl ester 
• 84230-81-9 Benzoic acid (2E,4E,6Z,9Z)-1-(4-methoxycarbonyl-butyl)-pentadeca-2,4,6,9-tetraenyl ester 
• 84230-79-5 Benzoic acid (2E,4E)-6-acetoxy-1-(4-methoxycarbonyl-butyl)-6-phenylsulfanyl-hexa-2,4-dienyl ester 
• 84230-78-4 Benzoic acid (2E,4E)-6-benzenesulfinyl-1-(4-methoxycarbonyl-butyl)-hexa-2,4-dienyl ester 
• 84230-77-3 Benzoic acid (E)-2-benzenesulfinyl-1-(4-methoxycarbonyl-butyl)-hexa-3,5-dienyl ester 
• 84230-80-8 Benzoic acid (2E,4E)-1-(4-methoxycarbonyl-butyl)-6-oxo-hexa-2,4-dienyl ester 

Relevant academic research and scientific papers

Adaptation of the photo-induced [1,3]-allylic phenylthio shift to the preparation of functionalized diquinanes

The feasibility of utilizing the little known photo-induced [1,3]- allylic phenylthio shift in the context of functionalized diquinane construction has been tested.

SYNTHESE NEUER ORGANOELEMENTSUBSTITUIERTER PENTADIENE (1)

By applying four different methods twelve new organoelement substituted pentadienes have been prepared.They contain one or two organoelement groups. - Pentadienyllithium (2) reacted with Cl-SPh, Br-SePh, Cl-PPh2, and Cl-AsPh2 (lone pair at the element) ex

TOTAL SYNTHESIS OF 5-DESOXYLEUKOTRIENE D. A NEW AND USEFUL EQUIVALENT OF THE 4-FORMYL-TRANS,TRANS-1,3-BUTADIENYL ANION

The first total synthesis of 5-desoxyleukotriene D (14) is reported.The route of synthesis utilizes a novel method for five-carbon chain extension.The availability of 14 allowed experimental demonstration that the 5-hydroxyl function is important for biological activity of the slow reacting substances.