177329-62-3

Upstream product

• 184840-85-5 tert-Butyl (3S,αR)-(E)-3-[N-benzyl-N-(α-methylbenzyl)amino]hex-4-enoate 
• 5933-40-4 (R)-(+)-N,α-dimethylbenzylamine 
• 81838-85-9 tert-butyl (2E,4E)-2,4-hexadienoate 

Downstream Products

• 178102-05-1 (5R,αR)-(E)-5-hex-3-en-1-ol 
• 177329-67-8 (6R,αR)-2-Methyl-6-hept-2-ene 
• 177329-65-6 (6R,αR)-(E)-2-Methyl-6-hept-4-en-2-ol 
• 177329-66-7 (6R,αR)-2-Methyl-6-heptan-2-ol 
• 177329-64-5 (4S,αR)-(E)-2-Methyl-4-hept-5-en-2-ol 
• 178102-04-0 (3S,αR)-(E)-3-hex-4-en-1-ol 
• 177329-63-4 (3S,αR)-(E)-Methyl 3-hex-4-enoate 

Relevant academic research and scientific papers

Asymmetric synthesis of (R)-hexane-1,5-diol and (R)-hex-3-ene-1,5-diol via a tandem asymmetric conjugate addition/stereospecific Meisenheimer rearrangement protocol

Stereoselective conjugate addition of (R)-lithium N,α-dimethylbenzylamide to tert-butyl (E,E)-hexa-2,4-dienoate, followed by reduction of the ester to the corresponding alcohol, affords a substrate which undergoes, on oxidation, a stereospecific Meisenheimer rearrangement to give a single diastereomer of the corresponding trialkylhydroxylamine. Cleavage of the N-O bond gives (R)-hex-3-ene-1,5-diol and subsequent hydrogenation of the double bond affords (R)-hexane-1,5-diol in high e.e.

Asymmetric synthesis of (R)-hexane-1,5-diol, (R)-hex-3-ene-1,5-diol and (R)-6-methylhept-5-en-2-ol (sulcatol) employing a tandem asymmetric conjugate addition and stereospecific Meisenheimer rearrangement protocol

Highly stereoselective conjugate addition of lithium (R)-N-methyl-(α-methylbenzyl)amide to tert-butyl (E,E)-hexa-2,4-dienoate, followed by reduction of the ester to the corresponding alcohol, affords a substrate which undergoes, upon oxidation, a stereospecific Meisenheimer rearrangement to give a single diastereomer of the corresponding trialkylhydroxylamine. The analogous N-benzyl adduct gives lower yields in the oxidation-rearrangement reaction. If the ester is not reduced to the alcohol, N-oxidation leads to Cope elimination, not Meisenheimer rearrangement. Cleavage of the N-O bond gives (R)-hex-3-ene-1,5-diol, and hydrogenation of the double bond affords (R)-hexane-1,5-diol in high ee. This methodology has been applied to the synthesis of the insect pheromone (R)-6-methylhept-5-en-2-ol (sulcatol) from tert-butyl (E,E)-hexa-2,4-dienoate, via a sequence involving conjugate addition of the lithium amide, Grignard addition to the ester, Meisenheimer rearrangement, hydrogenation of the double bond, dehydration of the tertiary alcohol and finally N-O bond cleavage.