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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 6, 1976 - Issue 8
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Original Articles

A General Synthetic Route to Optically Active Alkylpyridines from Alkylsubstituted Succinaldehyde Monoacetals

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Pages 549-554 | Received 10 Aug 1976, Published online: 05 Dec 2006

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G. Asara, C. Botteghi, S. Gladiali & F. Soccolini. (1983) A New Simple Synthesis of Optically Active Alkylpyridines: Remarks on the Maximum Rotatory Power of (+)-(S)-3-s. Butylpyridine. Synthetic Communications 13:13, pages 1129-1136.
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G. Caccia, G. Chelucci & C. Botteghi. (1981) Synthesis of (+)-(S)-4-s.Butyl and (+)-(S)-2-Methyl-4-s.Butylpyridine. Synthetic Communications 11:1, pages 71-83.
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C. Botteghi, G. Caccia, S. Gladiali & D. Tatone. (1979) A Simple Synthesis of an Optically Active Alkylvinylpyridine: (+)-(S)-2-Vinyl-5-sec. Butylpyridine. Synthetic Communications 9:2, pages 69-76.
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Articles from other publishers (7)

Cheng Chang, Frédéric Vogel, Oliver Kröcher & David Baudouin. (2024) The effect of Ni- and Mo-based materials on thermochemical sulfate reduction by glycerol under hydrothermal process conditions. Chemical Engineering Research and Design 205, pages 459-466.
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Meghan Fragis, Jackson L. Deobald, Srinivas Dharavath, Jeffrey Scott & Jakob Magolan. (2021) Aldehyde to Ketone Homologation Enabled by Improved Access to Thioalkyl Phosphonium Salts. Organic Letters 23:12, pages 4548-4552.
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T. D. Bailey, G. L. Goe & E. F. V. Scriven. 1985. Chemistry of Heterocyclic Compounds. Chemistry of Heterocyclic Compounds 1 252 .
. 1984. Comprehensive Heterocyclic Chemistry. Comprehensive Heterocyclic Chemistry 629 689 .
G. Jones. 1984. Comprehensive Heterocyclic Chemistry. Comprehensive Heterocyclic Chemistry 395 510 .
C.P. Forbes, G.L. Wenteler & A. Wiechers. (1978) Further applications of endocyclic enamine-enone annulations. Tetrahedron 34:4, pages 487-490.
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C. BOTTEGHI, G. CACCIA & S. GLADIALI. (2016) ChemInform Abstract: A GENERAL SYNTHETIC ROUTE TO OPTICALLY ACTIVE ALKYLPYRIDINES FROM ALKYL SUBSTITUTED SUCCINALDEHYDE MONOACETALS. Chemischer Informationsdienst 8:25.
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