A stereoselective method for the construction of the C8′–O–C6″ ether of nigricanoside-A: synthesis of simple models for the C20 lipid chain/galactosyl glycerol segment

Kinashi, Naoto; Fujiwara, Kenshu; Tsunoda, Takayuki et al.

Tetrahedron Letters, 2013, 54(34), 4564-4567

Permalink : https://hdl.handle.net/2115/58265

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アクセス権	open access
URI	https://hdl.handle.net/2115/58265
タイトル	A stereoselective method for the construction of the C8′–O–C6″ ether of nigricanoside-A: synthesis of simple models for the C20 lipid chain/galactosyl glycerol segment
著者	Kinashi, Naoto ; Fujiwara, Kenshu ; Tsunoda, Takayuki ; Katoono, Ryo ; Kawai, Hidetoshi ; Suzuki, Takanori
著者名 Kinashi, Naoto
e-Rad_Researcher 20222268 著者名 Fujiwara, Kenshu
著者名 Tsunoda, Takayuki
著者名 Katoono, Ryo
著者名 Kawai, Hidetoshi
e-Rad_Researcher 70202132 著者名 Suzuki, Takanori
言語	英語
キーワード	Natural product synthesis
	Monogalactosyl diacyl glycerol
	Ireland–Claisen rearrangement
	Ether lipid
	Stereoselective synthesis
発行日	2013-08-21
出版者	Elsevier
収録物名	Tetrahedron Letters
巻(号)	54(34)
ページ	4564-4567
抄録	A method for the stereoselective construction of the C8′–O–C6″ ether of nigricanoside-A, an antimitotic natural product from the green alga Avrainvillea nigricans, has been developed based on chirality-transferring Ireland–Claisen rearrangement. The method was successfully applied to the synthesis of simple models for the C20 lipid chain/galactosyl glycerol segment of the natural product.
資源タイプ	学術雑誌論文
出版タイプ	Accepted Manuscript
PISSN	0040-4039
関連情報 (isVersionOf)	出版社版DOI https://doi.org/10.1016/j.tetlet.2013.06.085