том 39 издание 43

ChemInform Abstract: Catalytic Enantioselective Reformatsky Reactions

Тип публикацииJournal Article
Дата публикации2008-10-21
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ISSN09317597, 15222667
General Medicine
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The Reformatsky reaction is a venerable named reaction that was introduced more than 120 years ago. Diastereoselective variants based on the use of chiral auxiliary and enantioselective protocols, based on the employment of stoichiometric amount of chiral lig- ands, have been successfully applied in organic synthesis during the years. However, a facile and general catalytic enantioselective variant was still a difficult task. Recently, we have es- tablished a new general and straightforward methodology for catalytic enantioselective Reformatsky reaction based on different concepts. In this paper, we present our general find- ing in catalytic enantioselective Reformatsky reaction of ketones, imines, and aldehydes. Our simple methodologies could become benchmark reactions for testing new synthesized chiral ligands for asymmetric transformations.

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Cozzi P. G., Mignogna A., Zoli L. ChemInform Abstract: Catalytic Enantioselective Reformatsky Reactions // ChemInform. 2008. Vol. 39. No. 43.
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Cozzi P. G., Mignogna A., Zoli L. ChemInform Abstract: Catalytic Enantioselective Reformatsky Reactions // ChemInform. 2008. Vol. 39. No. 43.
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TY - JOUR
DO - 10.1002/chin.200843250
UR - https://doi.org/10.1002/chin.200843250
TI - ChemInform Abstract: Catalytic Enantioselective Reformatsky Reactions
T2 - ChemInform
AU - Cozzi, Pier Giorgio
AU - Mignogna, Alessandro
AU - Zoli, Luca
PY - 2008
DA - 2008/10/21
PB - Wiley
IS - 43
VL - 39
SN - 0931-7597
SN - 1522-2667
ER -
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@article{2008_Cozzi,
author = {Pier Giorgio Cozzi and Alessandro Mignogna and Luca Zoli},
title = {ChemInform Abstract: Catalytic Enantioselective Reformatsky Reactions},
journal = {ChemInform},
year = {2008},
volume = {39},
publisher = {Wiley},
month = {oct},
url = {https://doi.org/10.1002/chin.200843250},
number = {43},
doi = {10.1002/chin.200843250}
}
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