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Ca++-modulators. Unusual highly stereospecific hantzsch-like cyclization: first authenticated example of 2-chloromethylene-1,2,3,4-tetrahydropyridine

✍ Scribed by M. Frigerio; A. Zaliani; C. Riva; G. Palmisano; T. Pilati; C.A. Gandolfi


Publisher
Elsevier Science
Year
1988
Tongue
French
Weight
260 KB
Volume
29
Category
Article
ISSN
0040-4039

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✦ Synopsis


Hantzsch cyclization of ethyl 4chloro-2-benzylidene-acetoacetates 5 with methyl 3-aminocrotonate 6 leads to 2chloromethylene-l,2,3,4-tetrahydropyridine-3,5-dicarboxylic esters 2. X-ray structure analysis and 'H-NMR of 7a established the configuration at Cs-C, as m, with borh the two bulky