期刊
SYNLETT
卷 -, 期 13, 页码 2051-2067出版社
GEORG THIEME VERLAG KG
DOI: 10.1055/s-0029-1217511
关键词
lanthanides; samarium diiodide; catalysis; enantio-selectivity; carbon-nitrogen bond formation
资金
- CNRS
- Ministere de l'Enseignement Superieur et de la Recherche
Lanthanide iodides offer great reactive scope as Lewis acid catalysts. Samarium diiodide allows a wide range of carbon-carbon bond-forming reactions, such as Mukaiyama aldol, Diels-Alder, or tandem Mukaiyama Michael aldol reactions. Moreover, lanthanide iodides exhibit high catalytic activities for carbon-nitrogen bond formations which are reviewed here. Highly enantio-enriched amino alcohol and amino acid building blocks are obtained thanks to a new family of enantioselective catalysts developed in our laboratory, iodolanthanide binaphtholates.
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