2024-03-29T10:57:46Zhttps://repositori.uji.es/oai/requestoai:repositori.uji.es:10234/933972023-01-26T10:32:57Zcom_10234_7053com_10234_9col_10234_8639
Repositori UJI
author
Escorihuela, Jorge
author
Burguete, M. Isabel
author
Luis, Santiago V.
2014-05-23T09:41:46Z
2014-05-23T09:41:46Z
2013-04-16
Escorihuela, J., Burguete, M. I., & Luis, S. V. (2013). New advances in dual stereocontrol for asymmetric reactions. Chemical Society Reviews, 42(12), 5595-5617
http://hdl.handle.net/10234/93397
http://dx.doi.org/10.1039/C3CS60068H
Achieving dual stereocontrol in asymmetric reactions using a single enantiomer for the building of the chiral catalyst or auxiliary is a very important goal in enantioselective synthesis as it eliminates the need for having available the two enantiomers of the auxiliary or catalyst designed. Recent strategies and advances towards this goal during the last four years will be discussed throughout this review.
eng
This journal is © The Royal Society of Chemistry 2013
Friedel-crafts alkylation
Diels-alder reactions
Alpha-amino amides
C(2)-SYMMETRIC COPPER(II) COMPLEXES
1,3-DIPOLAR CYCLOADDITION REACTIONS
ENANTIOSELECTIVE ALDOL ADDITIONS
MANNICH-TYPE REACTIONS
SINGLE CHIRAL SOURCE
CONJUGATE ADDITION
MN-III(SALEN)-CATALYZED EPOXIDATION
New advances in dual stereocontrol for asymmetric reactions
info:eu-repo/semantics/article
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