Asymmetric Michael addition of malonates to enones catalyzed by a siloxy amino acid lithium salt


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Please use this identifier to cite or link to this item:http://hdl.handle.net/2115/40078

Title:	Asymmetric Michael addition of malonates to enones catalyzed by a siloxy amino acid lithium salt
Authors:	Yoshida, Masanori Browse this author →KAKEN DB
	Narita, Mao Browse this author
	Hirama, Keisuke Browse this author
	Hara, Shoji Browse this author
Issue Date:	30-Dec-2009
Publisher:	Elsevier Ltd.
Journal Title:	Tetrahedron Letters
Volume:	50
Issue:	52
Start Page:	7297
End Page:	7299
Publisher DOI:	10.1016/j.tetlet.2009.10.033
Abstract:	Siloxy amino acid lithium salt, O-tert-butyldiphenylsilyl L-serine lithium salt, was found to be an effective catalyst for the asymmetric Michael addition reaction of malonates to enones.
Type:	article (author version)
URI:	http://hdl.handle.net/2115/40078
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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