Molecular Iodine-Catalyzed Imino-Diels-Alder Reactions: Efficient One-Pot Synthesis of Pyrano[3,2-c]quinolines
Тип публикации: Journal Article
Дата публикации: 2005-09-07
scimago Q3
wos Q3
БС2
SJR: 0.437
CiteScore: 3.3
Impact factor: 1.4
ISSN: 09365214, 14372096
Organic Chemistry
Краткое описание
The successful use of molecular iodine as a catalyst in the intermolecular imino-Diels-Alder reaction is described. A one-pot synthesis of pyrano[3,2-c]quinolines was achieved by three-component coupling of aldehydes and anilines with 2,3-dihydropyran catalyzed by iodine. The reactions could be carried out smoothly at room temperature within three to six hours to offer the target products in good yields. We also investigated solvent effect, substituent effect, and the amount of iodine required.
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Xia M., Lu Y. D. Molecular Iodine-Catalyzed Imino-Diels-Alder Reactions: Efficient One-Pot Synthesis of Pyrano[3,2-c]quinolines // Synlett. 2005. Vol. 15. pp. 2357-2361.
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Xia M., Lu Y. D. Molecular Iodine-Catalyzed Imino-Diels-Alder Reactions: Efficient One-Pot Synthesis of Pyrano[3,2-c]quinolines // Synlett. 2005. Vol. 15. pp. 2357-2361.
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TY - JOUR
DO - 10.1055/s-2005-872676
UR - https://doi.org/10.1055/s-2005-872676
TI - Molecular Iodine-Catalyzed Imino-Diels-Alder Reactions: Efficient One-Pot Synthesis of Pyrano[3,2-c]quinolines
T2 - Synlett
AU - Xia, Min
AU - Lu, Yue Dong
PY - 2005
DA - 2005/09/07
PB - Georg Thieme Verlag KG
SP - 2357-2361
IS - 15
SN - 0936-5214
SN - 1437-2096
ER -
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@article{2005_Xia,
author = {Min Xia and Yue Dong Lu},
title = {Molecular Iodine-Catalyzed Imino-Diels-Alder Reactions: Efficient One-Pot Synthesis of Pyrano[3,2-c]quinolines},
journal = {Synlett},
year = {2005},
publisher = {Georg Thieme Verlag KG},
month = {sep},
url = {https://doi.org/10.1055/s-2005-872676},
number = {15},
pages = {2357--2361},
doi = {10.1055/s-2005-872676}
}