Molecules 2000, 5(8), 1051-1054; doi:10.3390/50801051
Article

Convenient Synthesis of (3R, 4S)-4-Methyl-3-hexanol and (S)-4-Methyl-3-hexanone, the Pheromones of Ants

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Received: 3 April 2000; in revised form: 28 July 2000 / Accepted: 1 August 2000 / Published: 28 August 2000
This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Abstract: Synthesis of enantiopure pheromones I and II, both of them bearing chiral methyl branching and an α-oxygenated carbon centre, has been accomplished using compound 2 prepared from D-mannitol as the chiral precursor.
Keywords: pheromones; chiral methyl branching; (R)-2; 3-cyclohexylideneglyceraldehyde; a-oxygenated carbon centre
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MDPI and ACS Style

Dhotare, B.; Hassarajani, S.A.; Chattopadhyay, A. Convenient Synthesis of (3R, 4S)-4-Methyl-3-hexanol and (S)-4-Methyl-3-hexanone, the Pheromones of Ants. Molecules 2000, 5, 1051-1054.

AMA Style

Dhotare B, Hassarajani SA, Chattopadhyay A. Convenient Synthesis of (3R, 4S)-4-Methyl-3-hexanol and (S)-4-Methyl-3-hexanone, the Pheromones of Ants. Molecules. 2000; 5(8):1051-1054.

Chicago/Turabian Style

Dhotare, B.; Hassarajani, S. A.; Chattopadhyay, A. 2000. "Convenient Synthesis of (3R, 4S)-4-Methyl-3-hexanol and (S)-4-Methyl-3-hexanone, the Pheromones of Ants." Molecules 5, no. 8: 1051-1054.

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