1333236-98-8

Upstream product

• 18162-48-6 tert-butyldimethylsilyl chloride 
• 87727-28-4 (S)-2-tert-butyl-dimethyl-silanyloxy propanal 
• 105198-38-7 ethyl (S)-2-(tert-butyldimethylsilyloxy)propanoate 
• 1333236-95-5 (4R,5S)-4-(benzyloxy)-5-[(tert-butyldimethylsilyl)oxy]hexan-1-ol 
• 1333236-88-6 (5S,6R)-6-(benzyloxy)-2,2,3,3,5,11,11,12,12-nonamethyl-4,10-dioxa-3,11-disilatridecane 
• 1333236-84-2 (5S,6R)-2,2,3,3,5,11,11,12,12-nonamethyl-4,10-dioxa-3,11-disilatridecan-6-ol 

Downstream Products

• 1333237-65-2 C₃₅H₅₉ClO₆Si₂ 
• 1333237-02-7 ((2S,3S)-3-((1R,2S,4S,9R,10S,z)-9-(benzyloxy)-4,10-bis(tert-butyldimethylsilyloxy)-1,2-dichloroundec-5-enyl)oxiran-2-yl)methyl acetate 
• 1333237-05-0 ((2S,3S)-3-((1R,2S,4S,5R,6R,9R,10S)-9-(benzyloxy)-4,10-bis(tert-butyldimethylsilyloxy)-1,2,5,6-tetrachloroundecyl)oxiran-2-yl)methyl acetate 
• 1333237-00-5 ((4R,5S)-4-(benzyloxy)-5-(tert-butyldimethylsilyloxy)hexyl)triphenylphosphonium iodide 

Relevant academic research and scientific papers

Synthesis of undecachlorosulfolipid A: Re-evaluation of the nominal structure

Halo-giant: The title compound at the left in the scheme was constructed by the synthesis and coupling of two stereochemically challenging fragments. A comparison of the NMR data of the synthetic material and the natural product indicates that the configuration had been misassigned in the latter. PT=5-(1-phenyltetrazolyl).