1354770-15-2

Upstream product

• 58479-61-1 tert-butylchlorodiphenylsilane 
• 121671-76-9 5-(tert-butyldiphenylsilyloxy)pentan-1-ol 
• 131216-47-2 5-(tert-butyldiphenylsilyloxy)pentanal 
• 111-29-5 1 ,5-pentanediol 
• 1333237-23-2 5-(tert-butyldiphenylsilyloxy)-2,2-dichloropentanal 
• 1333237-29-8 (2S,3S,4R)-1-(benzyloxy)-8-((tert-butyldiphenylsilyl)oxy)-3,5,5-trichlorooctane-2,4-diol 
• 26164-26-1 (S)-2-methoxy-2-phenylacetic acid 
• 1333237-28-7 (2S,3S)-1-(benzyloxy)-8-(tert-butyldiphenylsilyloxy)-3,5,5-trichloro-2-hydroxyoctan-4-one 
• 1333237-27-6 1-((2R,3S)-3-((benzyloxy)methyl)oxiran-2-yl)-5-((tert-butyldiphenylsilyl)oxy)-2,2-dichloropentan-1-one 
• 1333237-26-5 (R)-1-((2S,3S)-3-(benzyloxymethyl)oxiran-2-yl)-5-(tert-butyldiphenylsilyloxy)-2,2-dichloropentan-1-ol 
• 1333237-25-4 (R,e)-1-(benzyloxy)-8-(tert-butyldiphenylsilyloxy)-5,5-dichlorooct-2-en-4-ol 
• 1333237-24-3 (R)-1-(benzyloxy)-8-(tert-butyldiphenylsilyloxy)-5,5-dichlorooct-2-yn-4-ol 

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).