119841-69-9

Upstream product

• 100-39-0 benzyl bromide 
• 58479-61-1 tert-butylchlorodiphenylsilane 
• 98-88-4 benzoyl chloride 

Downstream Products

• 119841-65-5 (R)-5-{(S)-[(2S,3S,4S)-3-Benzyloxy-4-(tert-butyl-diphenyl-silanyloxy)-tetrahydro-furan-2-yl]-methoxy-methyl}-5-methyl-dihydro-furan-2-one 
• 119841-65-5 (S)-5-{(S)-[(2S,3S,4S)-3-Benzyloxy-4-(tert-butyl-diphenyl-silanyloxy)-tetrahydro-furan-2-yl]-methoxy-methyl}-5-methyl-dihydro-furan-2-one 
• 119841-64-4 (1S,2S)-1-[(2S,3S,4S)-3-Benzyloxy-4-(tert-butyl-diphenyl-silanyloxy)-tetrahydro-furan-2-yl]-1-methoxy-2-methyl-hex-5-en-2-ol 
• 119841-64-4 (1S,2R)-1-[(2S,3S,4S)-3-Benzyloxy-4-(tert-butyl-diphenyl-silanyloxy)-tetrahydro-furan-2-yl]-1-methoxy-2-methyl-hex-5-en-2-ol 
• 114158-43-9 (1R,2R,3S,6R,7S,8S)-3-(tert-Butyl-diphenyl-silanyloxy)-2-hydroxy-7-methoxy-8-methyl-5,9-dioxa-tricyclo[6.2.1.0^2,6]undecan-10-one 
• 114247-53-9 (1S,2R,3S,6R,7S,8R)-3-(tert-Butyl-diphenyl-silanyloxy)-2-hydroxy-7-methoxy-8-methyl-5,9-dioxa-tricyclo[6.2.1.0^2,6]undecan-10-one 
• 114158-41-7 C₂₇H₃₄O₆Si 
• 114158-41-7 C₂₇H₃₄O₆Si 
• 119841-63-3 (S)-1-[(2S,3S,4S)-3-Benzyloxy-4-(tert-butyl-diphenyl-silanyloxy)-tetrahydro-furan-2-yl]-1-methoxy-propan-2-one 
• 119841-62-2 (S)-[(2S,3S,4S)-3-Benzyloxy-4-(tert-butyl-diphenyl-silanyloxy)-tetrahydro-furan-2-yl]-methoxy-acetaldehyde 
• 119841-61-1 Benzoic acid (R)-2-[(2R,3S,4S)-3-benzyloxy-4-(tert-butyl-diphenyl-silanyloxy)-tetrahydro-furan-2-yl]-2-methoxy-ethyl ester 

Relevant academic research and scientific papers

Synthesis of the Optically Active Hexahydrobenzofuran Nucleus of the Avermectins

A preparation of an optically pure hexahydrobenzofuranone subunit common to the milbemycin-avermectin macrocycles is reported from 1,4-anhydrosorbitol.