842141-75-7

Upstream product

• 824-94-2 p-methoxybenzyl chloride 
• 842141-74-6 (S)-2-Benzyloxy-1-((2R,4S,5S,6R)-5-methyl-4-triisopropylsilanyloxy-6-triisopropylsilanyloxymethyl-tetrahydro-pyran-2-yl)-ethanol 
• 842141-59-7 (S)-2-Benzyloxy-1-((2R,4S,5S,6R)-6-hydroxymethyl-5-methyl-4-triisopropylsilanyloxy-tetrahydro-pyran-2-yl)-ethanol 
• 842141-58-6 [(1S,2S)-1-((2S,3R)-3-Benzyloxymethyl-oxiranylmethyl)-2-((R)-2,2-dimethyl-[1,3]dioxolan-4-yl)-propoxy]-triisopropyl-silane 
• 842141-53-1 (2R,3S,4S)-6-(tert-Butyl-dimethyl-silanyloxy)-3-methyl-4-triisopropylsilanyloxy-hexane-1,2-diol 
• 842141-56-4 (Z)-(5S,6S)-6-((R)-2,2-Dimethyl-[1,3]dioxolan-4-yl)-5-triisopropylsilanyloxy-hept-2-enoic acid methyl ester 
• 842141-84-8 {(2R,3S)-3-[(2S,3S)-3-((R)-2,2-Dimethyl-[1,3]dioxolan-4-yl)-2-triisopropylsilanyloxy-butyl]-oxiranyl}-methanol 
• 842141-57-5 (Z)-(5S,6S)-6-((R)-2,2-Dimethyl-[1,3]dioxolan-4-yl)-5-triisopropylsilanyloxy-hept-2-en-1-ol 
• 842141-72-4 (3S,4S)-6-(tert-Butyl-dimethyl-silanyloxy)-3-methyl-4-triisopropylsilanyloxy-hex-1-ene 
• 842141-55-3 (3S,4S)-4-((R)-2,2-Dimethyl-[1,3]dioxolan-4-yl)-3-triisopropylsilanyloxy-pentanal 
• 756834-72-7 (3S,4S)-3-methyl-6-<(tert-butyldimethylsilyl)oxy>-1-hexen-4-ol 

Downstream Products

• 842141-61-1 (2R,3R,4S,6R)-6-[(S)-2-Benzyloxy-1-(4-methoxy-benzyloxy)-ethyl]-2-hydroxymethyl-3-methyl-tetrahydro-pyran-4-ol 
• 842141-76-8 (2R,3R,4S,6R)-6-[(S)-2-Benzyloxy-1-(4-methoxy-benzyloxy)-ethyl]-3-methyl-2-triisopropylsilanyloxymethyl-tetrahydro-pyran-4-ol 

Relevant academic research and scientific papers

Studies toward the total synthesis of sorangicins: Asymmetric synthesis of the key fragments

Efficient synthesis of the key fragments of the complex antibiotics class of sorangicins (Scheme 1) is described. Starting from simple compounds fragments I, II, and IV can be synthesized. For fragment III we chose an approach via L-glucal.