845508-87-4

Upstream product

• 1360570-80-4 ethyl-3-(tert-butyldimethylsilyloxy)-2-methylene-5-phenylpentanoate 
• 1226543-99-2 ethyl-3-hydroxy-2-methylene-5-phenylpentanoate 
• 104-53-0 3-phenyl-propionaldehyde 
• 845508-85-2 acetic acid 3-[(tert-butyl)(dimethyl)silanyloxy]-2-methylidene-5-phenyl-pentyl ester 
• 235090-81-0 Acetic acid 3-hydroxy-2-methylene-5-phenyl-pentyl ester 
• 18162-48-6 tert-butyldimethylsilyl chloride 
• 845508-86-3 3-[(tert-butyl)(dimethyl)silanyloxy]-2-methylidene-5-phenylpentanol 

Downstream Products

• 845508-88-5 Z-(tert-butyl)(dimethyl)(2-methylidene-1-phenethyl-oct-3-enyloxy)silane 
• 1360570-89-3 3-(tert-butyldimethylsilyloxy)-4-methylene-1-phenylnonan-5-ol 
• 1360570-90-6 4-(tert-butyldimethylsilyloxy)-3-methylene-1,6-diphenylhexan-2-ol 
• 1360570-69-9 (E)-(9-(4-methoxybenzyloxy)-4-pentyl-1-phenylnon-4-ene-3-yloxy)(tert-butyl)dimethylsilane 
• 1360570-67-7 (E)-tert-butyl(4-isobutyl-1,6-diphenylhex-4-ene-3-yloxy)dimethylsilane 
• 1360570-66-6 (E)-tert-butyldimethyl(4-pentyl-1,6-diphenylhex-4-ene-3-yloxy)silane 
• 1360570-65-5 (E)-tert-butyl(4-isobutyl-1-phenylnon-4-ene-3-yloxy)dimethylsilane 
• 1360570-64-4 (E)-tert-butyldimethyl(4-pentyl-1-phenylnon-4-ene-3-yloxy)silane 
• 1360571-02-3 9-(4-methoxybenzyloxy)-3-(tert-butyldimethylsilyloxy)-4-methylene-1-phenylnonan-5-yl 2-(diphenylphosphanyl)benzoate 
• 1360571-00-1 4-(tert-butyldimethylsilyloxy)-3-methylene-1,6-diphenylhexan-2-yl 2-(diphenylphosphino)benzoate 
• 1360570-99-5 3-(tert-butyldimethylsilyloxy)-4-methylene-1-phenylnonan-5-yl 2-(diphenylphosphanyl)benzoate 
• 143140-88-9 (tert-butyl)(dimethyl)(2-methylidene-1-phenethyl-but-3-enyloxy)silane 
• 845508-89-6 Z-(tert-butyl)(dimethyl)(2-methylidene-1-phenethyl-pent-3-enyloxy)silane 

Relevant academic research and scientific papers

Stereoselective and diversity-oriented synthesis of trisubstituted allylic alcohols and amines

Stereoselective and diversity-oriented synthesis of trisubstituted olefins was achieved by using ortho-diphenylphosphanyl benzoate (o-DPPB) as a directing group for allylic substitution. The starting point of this methodology was a set of α-methylene alde

Equilibrium control in enyne metathesis: Crossover studies and the kinetic reactivity of (E,Z)-1,3-disubstituted-1,3-dienes

(Chemical Equation Presented) The stereoselectivity of diene bond formation in the ruthenium-carbene mediated intermolecular enyne metathesis was studied. Initial reaction between an alkyne and 1-hexene gave mixtures of E- and Z-isomers in the newly forme