1027505-70-9

Upstream product

• 98-88-4 benzoyl chloride 
• 1028295-80-8 Benzoic acid (2S,3S)-3-azido-3-[(1S,2R)-1-(tert-butyl-diphenyl-silanyloxymethyl)-2-hydroxy-3-(4-methoxy-benzyloxy)-propylcarbamoyl]-2-methoxymethoxy-propyl ester 
• 501954-69-4 Benzoic acid (2S,3R)-3-azido-4-(4-methoxy-benzyloxy)-2-methoxymethoxy-butyl ester 
• 501954-68-3 Benzoic acid (2S,3R)-3-azido-2-hydroxy-4-(4-methoxy-benzyloxy)-butyl ester 
• 501954-67-2 Benzoic acid (2S,3S)-3-azido-3-carboxy-2-methoxymethoxy-propyl ester 
• 501954-70-7 Benzoic acid (2S,3R)-3-azido-4-hydroxy-2-methoxymethoxy-butyl ester 
• 193893-12-8 (2R,3S)-3-Azido-4-(tert-butyl-diphenyl-silanyloxy)-1-(4-methoxy-benzyloxy)-butan-2-ol 
• 1026486-55-4 (2R,3S)-3-Amino-4-(tert-butyl-diphenyl-silanyloxy)-1-(4-methoxy-benzyloxy)-butan-2-ol 
• 58479-61-1 tert-butylchlorodiphenylsilane 
• 1025823-46-4 C₄₀H₄₆N₄O₉Si 

Downstream Products

• 1027557-45-4 C₄₁H₄₈N₂O₈Si 

Relevant academic research and scientific papers

Toward the assignment of liposidomycin stereochemistry: Synthesis of 1,4-diazepan-3-one analogues by reductive amination approach

Toward the assignment of liposidomycin stereochemistry, a stereocontrolled synthesis of the liposidomycin diazepanone ring system and two precursors, has been achieved. The NMR coupling constants of a 5-phenyl model compound closely related to the liposidomycin diazepanone degradation product.