Organotin(IV) enamines as selective reagents: Coupling with α-halocarbonyls for synthesis of substituted pyrroles
Тип публикации: Journal Article
Дата публикации: 1997-05-01
scimago Q3
wos Q3
БС2
SJR: 0.334
CiteScore: 3.2
Impact factor: 1.5
ISSN: 00404039, 18733581
Organic Chemistry
Drug Discovery
Biochemistry
Краткое описание
Effective coupling of tin enamines 1 and α-haloaldehydes 2 gave 2,4-disubstituted pyrroles in high yields at room temperature even under aqueous conditions. The reaction with 2-bromoacetophenone gave 3,4-disubstituted pyrroles, while the addition of HMPA changed the selectivity to afford the 2,4-isomer predominantly (27:73).
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Yasuda M. et al. Organotin(IV) enamines as selective reagents: Coupling with α-halocarbonyls for synthesis of substituted pyrroles // Tetrahedron Letters. 1997. Vol. 38. No. 18. pp. 3265-3266.
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YASUDA M., MORIMOTO J., Shibata I., Baba A. Organotin(IV) enamines as selective reagents: Coupling with α-halocarbonyls for synthesis of substituted pyrroles // Tetrahedron Letters. 1997. Vol. 38. No. 18. pp. 3265-3266.
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TY - JOUR
DO - 10.1016/S0040-4039(97)00598-4
UR - https://doi.org/10.1016/S0040-4039(97)00598-4
TI - Organotin(IV) enamines as selective reagents: Coupling with α-halocarbonyls for synthesis of substituted pyrroles
T2 - Tetrahedron Letters
AU - YASUDA, MAKOTO
AU - MORIMOTO, Junji
AU - Shibata, Ikuya
AU - Baba, Akio
PY - 1997
DA - 1997/05/01
PB - Elsevier
SP - 3265-3266
IS - 18
VL - 38
SN - 0040-4039
SN - 1873-3581
ER -
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@article{1997_Yasuda,
author = {MAKOTO YASUDA and Junji MORIMOTO and Ikuya Shibata and Akio Baba},
title = {Organotin(IV) enamines as selective reagents: Coupling with α-halocarbonyls for synthesis of substituted pyrroles},
journal = {Tetrahedron Letters},
year = {1997},
volume = {38},
publisher = {Elsevier},
month = {may},
url = {https://doi.org/10.1016/S0040-4039(97)00598-4},
number = {18},
pages = {3265--3266},
doi = {10.1016/S0040-4039(97)00598-4}
}
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MLA
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Yasuda, Makoto, et al. “Organotin(IV) enamines as selective reagents: Coupling with α-halocarbonyls for synthesis of substituted pyrroles.” Tetrahedron Letters, vol. 38, no. 18, May. 1997, pp. 3265-3266. https://doi.org/10.1016/S0040-4039(97)00598-4.