ChemInform Abstract: Organocatalytically Enantioselective Approach to Polysubstituted Tetrahydropyridines and Piperidines.
Тип публикации: Journal Article
Дата публикации: 2012-01-05
General Medicine
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A convenient and highly enantioselective method for assembly of functionalized 1,2,3,4,5-pentasubstituted tetrahydropyridines and piperidines was developed. This method relies on preparing the required enantiopure cyclic semi-acetals via an organocatalyzed Michael addition/cyclization cascade reaction of aldehydes and alpha-keto-alpha,beta-unsaturated esters, and subsequent reductive amination/condensation with primary amines.
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Fang Yu., Zhang X., Jiang Y. ChemInform Abstract: Organocatalytically Enantioselective Approach to Polysubstituted Tetrahydropyridines and Piperidines. // ChemInform. 2012. Vol. 43. No. 5.
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Fang Yu., Zhang X., Jiang Y. ChemInform Abstract: Organocatalytically Enantioselective Approach to Polysubstituted Tetrahydropyridines and Piperidines. // ChemInform. 2012. Vol. 43. No. 5.
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TY - JOUR
DO - 10.1002/chin.201205162
UR - https://doi.org/10.1002/chin.201205162
TI - ChemInform Abstract: Organocatalytically Enantioselective Approach to Polysubstituted Tetrahydropyridines and Piperidines.
T2 - ChemInform
AU - Fang, Yu
AU - Zhang, Xiaojing
AU - Jiang, Yongwen
PY - 2012
DA - 2012/01/05
PB - Wiley
IS - 5
VL - 43
SN - 0931-7597
SN - 1522-2667
ER -
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@article{2012_Fang,
author = {Yu Fang and Xiaojing Zhang and Yongwen Jiang},
title = {ChemInform Abstract: Organocatalytically Enantioselective Approach to Polysubstituted Tetrahydropyridines and Piperidines.},
journal = {ChemInform},
year = {2012},
volume = {43},
publisher = {Wiley},
month = {jan},
url = {https://doi.org/10.1002/chin.201205162},
number = {5},
doi = {10.1002/chin.201205162}
}
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