896110-69-3

Upstream product

• 154001-54-4 (1E,4'S)-3-[(tert-Butyldiphenylsilyl)oxy]-1-(2',2'-dimethyl-1',3'-dioxolan-4'-yl)-1-propene 
• 102355-63-5 5,6-O-isopropylidene-D-mannono-1,4-lactone 
• 58479-61-1 tert-butylchlorodiphenylsilane 
• 81703-93-7 methyl (2E)-3-[(4S)-2,2-dimethyl-1,3-dioxolan-4-yl]acrylate 
• 79060-23-4 (2E)-3-[(4S)-2,2-dimethyl-1,3-dioxolan-4-yl]prop-2-en-1-ol 
• 896110-40-0 (E)-(R)-5-(tert-butyldiphenylsilyloxy)pent-3-ene-1,2-diol 

Downstream Products

• 896110-41-1 acetic acid (E)-(R)-4-(tert-butyldiphenylsilyloxy)-1-(tert-butyldiphenylsilyloxymethyl)but-2-enyl ester 
• 896110-46-6 [(E)-(4S,6R)-11-benzyloxy-4-(tert-butyldiphenylsilyloxymethyl)-(6-methoxymethoxy)undec-2-en-7-ynyl]oxy-tert-butyldiphenylsilane 
• 896110-44-4 (E)-(S)-11-benzyloxy-1-(tert-butyldiphenylsilyloxy)-4-(tert-butyldiphenylsilyloxymethyl)undec-2-en-7-yn-6-one 
• 896110-65-9 11-benzyloxy-1-(tert-butyl-diphenyl-silanyloxy)-4-(tert-butyl-diphenyl-silanyloxymethyl)-undec-2-en-7-yn-6-ol 
• 896110-45-5 11-benzyloxy-1-(tert-butyl-diphenyl-silanyloxy)-4-(tert-butyl-diphenyl-silanyloxymethyl)-undec-2-en-7-yn-6-ol 
• 896110-63-7 6-(tert-butyl-diphenyl-silanyloxy)-3-(tert-butyl-diphenyl-silanyloxymethyl)-hex-4-enoic acid 
• 896110-64-8 6-(tert-butyl-diphenyl-silanyloxy)-3-(tert-butyl-diphenyl-silanyloxymethyl)-hex-4-en-1-ol 
• 896110-42-2 (E)-(S)-6-(tert-butyldiphenylsilyloxy)-3-(tert-butyldiphenylsilyloxymethyl)hex-4-enoic acid methyl ester 
• 896110-70-6 {(1S,4R)-3-[4-Benzyloxy-but-(Z)-ylidene]-4-methoxymethoxy-2-methylene-cyclopentylmethoxy}-tert-butyl-diphenyl-silane 
• 896110-43-3 (E)-(S)-6-(tert-butyldiphenylsilyloxy)-3-(tert-butyldiphenylsilyloxymethyl)hex-4-enal 
• 896110-47-7 ((2S,4R)-9'-benzyloxy-4'-methoxymethoxy-2'-vinyl-non-5'-ynyloxy)-tert-butyldiphenylsilane 

Relevant academic research and scientific papers

Evaluation of possible intramolecular [4+2] cycloaddition routes for assembling the central tetracyclic core of the potent marine antiinflammatory agent mangicol A

A plan for enantioselective construction of the mangicol A framework by means of intramolecular Diels-Alder cycloaddition is outlined. First to be assembled is the enantiopure cyclopentenecarboxylic acid 16. Of the several approaches targeting the 1,3-die