214960-55-1

Upstream product

• 214960-50-6 (S)-5-(4-Methoxy-benzyloxy)-7-(2-methoxy-ethoxymethoxy)-hept-2-ynoic acid methyl ester 
• 214960-49-3 1-Methoxy-4-{(S)-1-[2-(2-methoxy-ethoxymethoxy)-ethyl]-but-3-ynyloxymethyl}-benzene 
• 80783-14-8 1-phenylmercapto-2,2-dimethyl-butan-3-one 
• 214960-48-2 (S)-1-(2-Methoxy-ethoxymethoxy)-hex-5-yn-3-ol 
• 214960-47-1 (R)-2-[2-(2-Methoxy-ethoxymethoxy)-ethyl]-oxirane 
• 7205-91-6 phenylthiomethyl chloride 
• 17510-44-0 (1,2-dimethyl-propenyloxy)-trimethyl-silane 
• 214960-41-5 Acetic acid 2,2-dimethyl-1-methylene-3-phenylsulfanyl-propyl ester 
• 214960-54-0 [(E)-(R)-3-Bromo-5-(4-methoxy-benzyloxy)-7-(2-methoxy-ethoxymethoxy)-hept-2-enyloxy]-tert-butyl-diphenyl-silane 

Relevant academic research and scientific papers

An approach to the C(17)-C(24) fragment of bryostatins: Applications of stereoselective trisubstituted alkene formation by palladium(0) catalysed coupling of enol acetates and vinylic bromides

The enol acetate 26 couples stereospecifically with the vinylic bromides 25 and 29 in the presence of tributyltin methoxide and a catalytic amount of dichlorobis(tri-o-tolylphosphine)palladium to give the βγ-unsaturated ketones 27 and 30 with retention of