53226-68-9

Upstream product

• 27200-84-6 methyl triphenylphosphonium bromide 
• 343771-16-4 (+/-)-(2R^*,3S^*)-2,3-Epoxy-2-methyl-3-phenylpropanal 
• 75-77-4 chloro-trimethyl-silane 
• 563-52-0 2-chloro-3-butene 
• 100-52-7 benzaldehyde 
• 1504-55-8 (E)-3-phenyl-2-methyl-2-propenol 
• 129313-31-1 (+/-)-(2S^*,3S^*)-2,3-Epoxy-2-methyl-3-phenylpropan-1-ol 

Downstream Products

• 25201-44-9 (1R,2S)-2-methyl-1-phenylbut-3-en-1-ol 
• 25201-44-9 (1R,2R)-2-methyl-1-phenylbut-3-en-1-ol 
• 116215-96-4 (1-methylcyclopropyl)(phenyl)methanol 
• 123290-15-3 2-butenyl-2-methyl-1-phenyl-1-ol 

Relevant academic research and scientific papers

Reactions of α-haloallyllithium derivatives with carbon, silicon, tin or boron halides and carbonyl compounds

A series of allylic halides have been converted into their α-carbanions with strong lithium bases, using different techniques.These have been compared in their reaction with various electrophiles leading to functionally substituted allyl derivatives.The influence of the counterion on the regio- and stereoselectivity has been investigated. allylic halides / α-halocarbanions / allylsilanes / allyltin derivatives / α-chlorohydrins / vinylepoxides / diastereoselectivity

Palladium-Catalyzed Selective Hydrogenolysis of Alkenyloxiranes with Formic Acid. Stereoselectivity and Synthetic Utility

Selective hydrogenolysis of alkenyloxiranes to give homoallylic alcohols was carried out using formic acid in the presence of palladium-phosphine catalyst.The selectivity of the reaction depends on a nature and an amount of phosphine ligands.The reaction