556068-55-4

Upstream product

• 42778-95-0 ethyl (E)-dodec-2-enoate 
• 17480-69-2 (S)-N-benzyl-1-phenylethylamine 
• 78217-11-5 dodec-2-enoic acid ethyl ester 
• 112-31-2 caprinaldehyde 

Downstream Products

• 602275-72-9 (4S,1'S)-4-(N-α-methylbenzyl-N'-benzylamino)-1-trimethylsilyl-2-(trimethylsilylmethyl)tridecan-2-ol 
• 556068-60-1 methyl (3S)-3-[(2-{[(1R)-1-benzyl-2-methoxy-2-oxoethyl]amino}-2-oxoethyl)amino]dodecanoate 
• 556068-63-4 methyl (3S)-3-[(2-{[(1S)-1-benzyl-2-methoxy-2-oxoethyl]amino}-2-oxoethyl)amino]dodecanoate 
• 556068-66-7 methyl (3S)-3-[(3S)-3-benzyl-2,5-dioxopiperazinyl]dodecanoate 
• 556068-64-5 methyl (3S)-3-[(3R)-3-benzyl-2,5-dioxopiperazinyl]dodecanoate 

Relevant academic research and scientific papers

Determination of the absolute stereochemistry of Etzionin

The absolute configuration of Etzionin, a marine peptide-like compound isolated in 1989 from a red tunicate collected from the Red Sea has been determined by a combination of synthetic and spectroscopic procedures. Finally, its absolute stereochemistry ha

A new asymmetric synthesis of 2,6-cis-disubstituted 4-methylenepiperidines: Total synthesis of (+)-alkaloid 241D and (+)-isosolenopsin A

A highly diastereoselective synthesis of 2,6-cis-disubstituted-4- methylenepiperidines based on a Mannich type intramolecular cyclization of an allylsilane on an iminium ion is described. The synthetic potential of this methodology is demonstrated by the

A facile enantioselective synthesis of 2-(2-aminoethyl)allylsilanes, new synthons for piperidine synthesis

The synthesis of chiral (2-substituted-2-aminoethyl)allylsilanes by cerium mediated trimethylsilylmethylmagnesium chloride addition to the ester group of non racemic chiral β-aminoesters is described.