1361022-98-1

Upstream product

• 1361022-93-6 (2R,6S,8S,3E)-1-benzyloxy-2,4,8-trimethylundec-3-en-6-ol 
• 1361022-94-7 (2R,6S,8S,3E)-2,4,8-trimethylundec-3-ene-1,6-diol 
• 1361022-95-8 (2R,6S,8S,3E)-2,4,8-trimethyl-1-(tri-isopropylsilyloxy)undec-3-en-6-ol 
• 1361022-96-9 (2R,4R,6S,8S)-2,4,8-trimethyl-1-(tri-isopropylsilyloxy)undecan-6-ol 
• 98-59-9 p-toluenesulfonyl chloride 
• 13231-81-7 (3S)-3-Methylhexan-1-ol 
• 110065-42-4 (3S)-3-methylhexanal 
• 7540-51-4 (S)-3,7-dimethyl-6-octen-1-ol 
• 13154-24-0 triisopropylsilyl chloride 
• 116370-25-3 (S)-tert-butyl ((3,7-dimethyloct-6-en-1-yl)oxy)dimethylsilane 
• 167834-10-8 (4S)-6-(tert-butyldimethylsilyloxy)-4-methyl-1-hexanol 

Downstream Products

• 1361023-07-5 [(7S,11RS,13R,15S,17R,19S)-7,13,15,17,19-pentamethyldocosan-11-yl](phenyl)sulfone 
• 1361023-08-6 [(7R,11RS,13R,15S,17R,19S)-7,13,15,17,19-pentamethyldocosan-11-yl]phenylsulfone 
• 1361023-09-7 (2R,4S,6R,8S)-2,4,6,8-tetramethylundecyl toluene p-sulfonate 

Relevant academic research and scientific papers

Systematic comparison of sets of 13C NMR spectra that are potentially identical. Confirmation of the configuration of a cuticular hydrocarbon from the cane beetle antitrogus parvulus

A systematic process is introduced to compare 13C NMR spectra of two (or more) candidate samples of known structure to a natural product sample of unknown structure. The process is designed for the case where the spectra involved can reasonably

Total synthesis of a cuticular hydrocarbon from the cane beetle Antitrogus parvulus: Confirmation of the relative stereochemistry

The stereoselective reaction of an allyl bromide with an aldehyde mediated by a low valency bismuth species was the key reaction in stereoselective syntheses of (4S,6R,8R,10S,16S)- and (4S,6R,8R,10S,16R)-4,6,8,10,16- pentamethyldocosanes. 13C N