Asymmetric Michael addition of aldehydes to nitroalkenes using a primary amino acid lithium salt


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Please use this identifier to cite or link to this item:http://hdl.handle.net/2115/45249

Title:	Asymmetric Michael addition of aldehydes to nitroalkenes using a primary amino acid lithium salt
Authors:	Yoshida, Masanori Browse this author
	Sato, Atsushi Browse this author
	Hara, Shoji Browse this author
Issue Date:	28-Jun-2010
Publisher:	Royal Society of Chemistry
Journal Title:	Organic & Biomolecular Chemistry
Volume:	8
Issue:	13
Start Page:	3031
End Page:	3036
Publisher DOI:	10.1039/c003940c
PMID:	20461274
Abstract:	Enantioselective Michael addition of aldehydes to nitroalkenes was successfully carried out by an asymmetric catalysis with L-phenylalanine lithium salt, giving γ-nitroaldehydes in good yields with high enantioselectivity.
Rights:	Org. Biomol. Chem., 2010, 8, 3031-3036 - Reproduced by permission of The Royal Society of Chemistry (RSC)
Type:	article (author version)
URI:	http://hdl.handle.net/2115/45249
Appears in Collections:	工学院・工学研究院 (Graduate School of Engineering / Faculty of Engineering) > 雑誌発表論文等 (Peer-reviewed Journal Articles, etc)

Submitter: 吉田雅紀

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