Stereocontrolled Total Synthesis of (+)- and (-)-Epibatidine

DOI: 10.1021/jo00073a013

Source and publish data:

Journal of Organic Chemistry p. 5600 - 5602 (1993)

Update date:2022-08-03

Topics:

Authors:

Corey, E. J.

Loh, Teck-Peng

AchyuthaRao, Sidduri

Daley, Donnette C.

Sarshar, Sepehr

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Article abstract of DOI:10.1021/jo00073a013

The stereocontrolled total synthesis of the novel analgesic agent (-)-epibatidine (1) and its enantiomer starting with 6-chloropyridine-3-carboxaldehyxe (2) has been carried out by way of intermediates 3-10.

Full text of DOI:10.1021/jo00073a013

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Article Doi

Stereocontrolled Total Synthesis of (+)- and (-)-Epibatidine

DOI: 10.1021/jo00073a013

Source and publish data:

Authors:

Article abstract of DOI:10.1021/jo00073a013

Full text of DOI:10.1021/jo00073a013

Products guided by the article

R&D Labs maybe for 152004-91-6

Relevant to this article

Furo-fused 2H-chromenes: Synthesis and photochromic properties

Accessing Alkyl- and Alkenylcyclopentanes from Cr-Catalyzed Ethylene Oligomerization Using 2-Phosphinophosphinine Ligands

Arylation of aryl chlorides, a convenient method for the synthesis of new potential triazolic fungicides

Neuroprotective activity of different monosaccharide-modified gastrodin analogs

Oxocarbons and Related Compounds. 20. By Thiophenols Mediated Conversion of Semisquaric Hydrazides to Squaric-1,2-Diamides

1H and 13C NMR spectral assignments of halogenated transformation products of pharmaceuticals and related environmental contaminants

¹H and ¹³C NMR spectral assignments of halogenated transformation products of pharmaceuticals and related environmental contaminants