867372-50-7

Upstream product

• 1006031-41-9 (E)-tert-butyl 6-(1-phenyl-1H-tetrazol-5-ylthio)hex-2-enoate 
• 4224-70-8 6-bromohexanoic acid 
• 65868-63-5 tert-butyl 6-bromohexanoate 
• 86-93-1 1-Phenyl-1H-tetrazole-5-thiol 

Downstream Products

• 867372-43-8 (8S,9S,10S)-11-(4-benzyl-2-oxooxazolidin-3-yl)-8-methoxy-9-methoxymethoxy-10-methyl-11-oxoundec-6-enoic acid tert-butyl ester 
• 867372-42-7 (8S,9S,10S)-11-(4-benzyl-2-oxooxazolidin-3-yl)-9-hydroxy-8-methoxy-10-methyl-11-oxoundec-6-enoic acid tert-butyl ester 
• 867372-38-1 6-(1-phenyl-1H-tetrazole-5-sulfonyl)hexanoic acid tert-butyl ester 

Relevant academic research and scientific papers

(BDP)CuH: A "hot" Stryker's reagent for use in achiral conjugate reductions

(Chemical Equation Presented) A ligand-modified, economical version of Stryker's reagent (SR) has been developed based on a bidentate, achiral bis-phosphine. Generated in situ, "(BDP)CuH" smoothly effects conjugate reductions of a variety of unsaturated substrates, including those that are normally unreactive toward SR. Substrate-to-ligand ratios typically on the order of 1000-10000:1 can be used leading to products in high yields.