38383-05-0

Upstream product

• 144121-60-8 1-phenylhex-5-en-1-ol 
• 1119-51-3 bromopentene 
• 100-52-7 benzaldehyde 

Downstream Products

• 1588-44-9 6-phenyl-1-hexene 
• 270901-39-8 2,2,6,6-tetramethyl-1-(1-phenylhex-5-enoyloxy)piperidine 
• 330938-07-3 N-tert-butyl-N-(2-methyl-1-phenylpropyl)-O-(1-phenylhex-5-enyl)hydroxylamine 
• 270901-83-2 N,N-di-tert-butyl-O-(1-phenyl-hex-5-enyl)-hydroxylamine 
• 853886-26-7 4-(tert-butyl-dimethyl-silanyloxy)-2,2,6,6-tetramethyl-1-(1-phenyl-hex-5-enyloxy)-piperidine 
• 853886-36-9 2,2,7,7-tetramethyl-1-(1-phenylhex-5-enyloxy)[1,4]diazepane-5-one 
• 853886-37-0 2,2,7,7-tetramethyl-1-(1-phenylhex-5-enyloxy)-azepane-4-one 
• 853886-44-9 2,2,6,6-tetraethyl-1-(1-phenylhex-5-enyloxy)-piperidin-4-ol 

Relevant academic research and scientific papers

Method for synthesizing alkyne through catalytic asymmetric cross coupling (by machine translation)

The invention belongs to the field of, asymmetric synthesis, and discloses a method for catalyzing asymmetric cross- coupling to synthesize: an alkyne, and the L method comprises, the following steps, of A: preparing B a cuprous, salt and C a: ligand; preparing a catalyst; adding a base; reacting the compound with the compound with the compound; and reacting the compound with the compound. Of these, one of them, X is selected from the group consisting of, R halogens. 1 Optionally substituted heteroarylsulfonylcyanamide groups selected from the, group consisting, of optionally substituted, phenyl groups In-flight vehicle, R6 Trialkyl silyl groups or alkyl radicals, R2 Cycloalkyl radicals optionally substituted with an, optionally substituted alkyl, (CH radical2 )n R4 Multi,layer chain, n＝0-10,R saw blade4 A group selected, from, the group consisting of phenyl, alkenyl, aralkynyls, noonyloxy,and, noonylsulfonylsulfonylsulfonylsulfonylsulfonylsulfonylsulfonylsulfonylsulfonylsulphonylsulphonylsulphonylsulphonylsulphonylsulphonylsulphonylsulphonylsulphonylsulphonylphenyl disiloxy-radicals. R3 A ligand, selected from hydrogen or any of the functional groups, is selected from the group consisting of, hydrogen and any L other functional group. The method, R disclosed by the, A invention has the, advantages of good catalytic, R ’ effect, wide application range. and high catalytic efficiency, and the, method disclosed by the, invention has the. advantages of good catalytic effect, wide application range and high catalytic efficiency. (by machine translation)

Occurrence of Electron Transfer in the Reduction of Organic Halides by LiAlH4 and AlH3

A variety of methods have been utilized to detect the occurrence of a single electron transfer pathway in the reduction of alkyl halides by LiAlH4 and AlH3, i.e., (1) product studies of reduction of cyclizable alkyl halides containing the 5-hexenyl group, (2) trapping of intermediate radicals by dicyclohexylphosphine and other trapping agents, (3) direct EPR observation of the trityl radical in the reduction of trityl bromide, and (4) stereochemical studies of the reduction of secondary halides by lithium aluminum deuteride.The extent of electron transfer was found to be a function of the solvent, the substrate, the leaving group, and the hydride reagent.For alkyl iodides, and to a lesser extent bromides, electron transfer was found to be the major reaction pathway; however, no evidence for electron transfer was found for the corresponding chlorides or tosylates.Reduction of (+)-2-octyl iodide by LiAlD4 was found to be much less stereospecific than the corresponding reduction of bromide, chloride, or tosylate, indicating intermediate radical formation in the reduction of the secondary iodide.