155430-52-7

Upstream product

• 73814-74-1 (Z)-(R)-5-Benzyloxy-4-methyl-pent-2-en-1-ol 
• 81470-75-9 (Z)-(R)-5-Benzyloxy-4-methyl-pent-2-enoic acid methyl ester 
• 155430-48-1 (E)-3-[(2S,3S)-3-((1S,2S,3R,4S,5S)-6-Benzyloxy-1,3,5-trimethyl-2,4-bis-triethylsilanyloxy-hexyl)-oxiranyl]-acrylic acid ethyl ester 
• 155430-46-9 (E)-3-[(2R,3R)-3-((1S,2S,3S)-4-Benzyloxy-1,3-dimethyl-2-triethylsilanyloxy-butyl)-oxiranyl]-acrylic acid ethyl ester 
• 155430-50-5 (E)-(4R,5R,6S,7S,8R,9S,10S)-11-Benzyloxy-5,7,9-trihydroxy-4,6,8,10-tetramethyl-undec-2-enoic acid ethyl ester 
• 155430-49-2 (E)-3-[(2S,3S)-3-((1R,2R,3R,4S,5S)-6-Benzyloxy-2,4-dihydroxy-1,3,5-trimethyl-hexyl)-oxiranyl]-acrylic acid ethyl ester 
• 618096-10-9 (E)-(4S,5R,6S)-7-Benzyloxy-4,6-dimethyl-5-triethylsilanyloxy-hept-2-enoic acid ethyl ester 
• 155613-08-4 (E)-(4S,5S,6S,7S,8S)-9-Benzyloxy-5,7-dihydroxy-4,6,8-trimethyl-non-2-enoic acid ethyl ester 
• 155430-47-0 (E)-3-[(2R,3R)-3-((1R,2S,3S)-4-Benzyloxy-2-hydroxy-1,3-dimethyl-butyl)-oxiranyl]-acrylic acid ethyl ester 
• 155488-74-7 (E)-(4S,5R,6S)-ethyl 7-benzyloxy-5-hydroxy-4,6-dimethyl-2-heptenoate 
• 155430-45-8 (2R,3R,4R,5S,6S)-7-benzyloxy-2,3-epoxy-5-triethylsilyloxy-4,6-dimethyl-1-heptanol 
• 155430-44-7 (E)-(4S,5R,6S)-7-benzyloxy-5-triethylsilyloxy-4,6-dimethyl-2-hepten-1-ol 
• 155430-43-6 (E)-(4R,5S,6S)-ethyl 7-benzyloxy-4,5-epoxy-6-methyl-2-heptenoate 
• 618096-09-6 (2S,3S)-3-((S)-2-benzyloxy-1-methylethyl)oxirane-2-carbaldehyde 

Downstream Products

• 155430-53-8 (3S,4R,5R,6S,7R,8R,9S,10S)-11-Benzyloxy-4,6,8,10-tetramethyl-5,7,9-tris-triethylsilanyloxy-undecane-1,3-diol 
• 155430-54-9 2,2-Dimethyl-propionic acid (3S,4R,5R,6S,7R,8R,9S,10S)-11-benzyloxy-3-hydroxy-4,6,8,10-tetramethyl-5,7,9-tris-triethylsilanyloxy-undecyl ester 

Relevant academic research and scientific papers

Highly stereoselective epoxidation of a 4-methyl-5- (triethylsilyl)oxyallyl alcohol system with m-chloroperoxybenzoic acid

Epoxidation of 4-methyl-5-(triethylsilyl)oxyallyl alcohol system with m- chloroperoxybenzoic acid (MCPBA) has been found to occur highly stereoselectively and in high yields from the opposite side of the C5 triethylsilyloxy group regardless of

Synthetic Studies on Polypropionate Antibiotics Based on the Stereospecific Methylation of γ,δ-Epoxy Acrylates by Trimethylaluminum. A Highly Stereoselective Construction of the Eight Contiguous Chiral Centers of Ansa-chains of Rifamycins

A highly stereoselective construction of the eight contiguous chiral centers of ansa-chains of rifamycins has been accomplished by the iterative use of the stereospecific methylation of γ,δ-epoxy acrylates by trimethylaluminum which was recently developed