Addition reactions of heterocyclic compounds. Part XXXVIII. Cycl[3,2,2]azines and indolizines from pyridines and methyl propiolate

Тип публикации: Journal Article
Дата публикации: 1968-01-01
Royal Society of Chemistry (RSC)
SJR: —
CiteScore: —
Impact factor: —
ISSN: 00224952
Organic Chemistry
Краткое описание
Pyridine and its 3- and 4-methyl- and 3,5-dimethyl-derivatives with methyl propiolate gave indolizines and cycl-[3,2,2]azine esters, identified largely from their mass, n.m.r., and u.v. spectra. The formation of these products is discussed. The cyclazine from pyridine has been degraded to 1-methylcycl[3,2,2]azine, the n.m.r. spectrum of which has been fully analysed. 4-Methylpyridine also gave 1,4-dihydro-1-(2-methoxycarbonyl-trans-vinyl)-4-(3-methoxycarbonylprop-2-enylidene)pyridine.
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Acheson R. M., ROBINSON D. A. Addition reactions of heterocyclic compounds. Part XXXVIII. Cycl[3,2,2]azines and indolizines from pyridines and methyl propiolate // Journal of the Chemical Society C Organic. 1968. p. 1633.
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Acheson R. M., ROBINSON D. A. Addition reactions of heterocyclic compounds. Part XXXVIII. Cycl[3,2,2]azines and indolizines from pyridines and methyl propiolate // Journal of the Chemical Society C Organic. 1968. p. 1633.
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TY - JOUR
DO - 10.1039/j39680001633
UR - https://doi.org/10.1039/j39680001633
TI - Addition reactions of heterocyclic compounds. Part XXXVIII. Cycl[3,2,2]azines and indolizines from pyridines and methyl propiolate
T2 - Journal of the Chemical Society C Organic
AU - Acheson, R. M.
AU - ROBINSON, D A
PY - 1968
DA - 1968/01/01
PB - Royal Society of Chemistry (RSC)
SP - 1633
SN - 0022-4952
ER -
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@article{1968_Acheson,
author = {R. M. Acheson and D A ROBINSON},
title = {Addition reactions of heterocyclic compounds. Part XXXVIII. Cycl[3,2,2]azines and indolizines from pyridines and methyl propiolate},
journal = {Journal of the Chemical Society C Organic},
year = {1968},
publisher = {Royal Society of Chemistry (RSC)},
month = {jan},
url = {https://doi.org/10.1039/j39680001633},
pages = {1633},
doi = {10.1039/j39680001633}
}