634613-77-7

Upstream product

• 58479-61-1 tert-butylchlorodiphenylsilane 
• 634613-76-6 (1-hydroxymethyl-undeca-3,9-diynyl)-carbamic acid tert-butyl ester 
• 24424-99-5 di-tert-butyl dicarbonate 
• 634613-75-5 2-tert-butoxycarbonylamino-dodeca-4,10-diynoic acid methyl ester 
• 112505-31-4 trimethyl(nona-1,7-diyn-1-yl)silane 
• 634613-74-4 1-bromo-nona-1,7-diyne 
• 93267-04-0 N-(tert-butoxycarbonyl)-L-3-iodoalanine methyl ester 
• 83182-85-8 1-(trimethylsilyl)-1,7-octadiyne 
• 2766-43-0 N-tert-butyloxycarbonyl-L-serine methyl ester 
• 871-84-1 1,7-Octadiyne 

Downstream Products

• 634613-79-9 [1-(tert-butyl-diphenyl-silanyloxymethyl)-3-(2-non-2-enoyl-cyclohex-1-enyl)-propyl]-carbamic acid tert-butyl ester 
• 634613-81-3 (3S,5R,7aS,11aS)-3-[[(tert-butyldiphenylsilyl)oxy]methyl]-5-hexyloctahydro-pyrrolo-1H-pyrrolo[2,1-j]quinolin-7(7aH)-one 
• 634613-78-8 [3-(2-acetyl-cyclohex-1-enyl)-1-(tert-butyl-diphenyl-silanyloxymethyl)-propyl]-carbamic acid tert-butyl ester 

Relevant academic research and scientific papers

Chemoselectivity of the Ruthenium-Catalyzed Hydrative Diyne Cyclization: Total Synthesis of (+)-Cylindricine C, D, and E

(Matrix presented) The chemoselectivity of the ruthenium-catalyzed hydrative diyne cylization is explored In an expeditious synthesis of the tricyclic alkaloids cylindricine C, D, and E.