73199-51-6

Upstream product

• 3238-98-0 3-phenylthio-1-bromopropane 
• 25179-23-1 dilithium isobutyrate 
• 79-31-2 isobutyric Acid 

Downstream Products

• 73199-62-9 ((2Z,6E,11E,13E)-3,8,8,11,14,18-Hexamethyl-nonadeca-2,6,11,13,17-pentaenyloxymethyl)-benzene 
• 73199-61-8 [(6E,10Z)-2-Benzenesulfonyl-12-benzyloxy-2-((E)-3,7-dimethyl-octa-2,6-dienyl)-5,5,10-trimethyl-dodeca-6,10-dienyl]-trimethyl-silane 
• 73199-60-7 (2Z,6E,13E)-1-benzyloxy-11-phenylsulphonyl-3,8,8,14,18-pentamethylnonadeca-2,6,13,17-tetraene 
• 73199-59-4 (2Z,6E)-1-benzyloxy-11-phenylsulphonyl-3,8,8-trimethylundeca-2,6-diene 
• 87957-22-0 moenocinol benzyl ether 
• 73199-53-8 5-phenylsulphonyl-2,2-dimethylpentan-1-al 
• 87957-21-9 Benzoic acid (Z)-2-benzenesulfonyl-1-(4-benzenesulfonyl-1,1-dimethyl-butyl)-7-benzyloxy-5-methyl-hept-5-enyl ester 
• 73199-52-7 5-phenylsulphonyl-2,2-dimethylpentan-1-ol 
• 87957-25-3 5-phenylthio-2,2-dimethylpentan-1-ol 

Relevant academic research and scientific papers

A Synthesis of Moenocinol

The fluoride-induced elimination of a β-silyl sulfone and the reductive elimination of a β-acyloxy sulfone are key olefin-forming reactions in a new synthesis of moenocinol .

Sulphone-based Elimination Reactions in Synthesis. Part 1. Moenocinol

The fluoride-induced elimination of a β-phenylsulphonylsilane and the reductive elimination of a β-oxysulphone are key olefin-forming reactions in a synthesis of moenocinol .