Synthetic Progress toward Azadirachtins. 2. Enantio- and Diastereoselective Synthesis of the Right-Wing Fragment of 11-epi-Azadirachtin I

CORC > 北京大学 > 化学与分子工程学院

	Synthetic Progress toward Azadirachtins. 2. Enantio- and Diastereoselective Synthesis of the Right-Wing Fragment of 11-epi-Azadirachtin I
	Tan Ceheng ; Chen Wei ; Mu Xinpeng ; Chen Qi ; Gong Jianxian ; Luo Tuoping ; Yang Zhen
刊名	organic letters
	2015
DOI	10.1021/acs.orglett.5b00831
英文摘要	A stereoselective three-component coupling reaction of allylzinc bromide, silyl glyoxylate, and a β-lactone has been developed. This has been successfully applied to the enantio- and diastereoselective synthesis of the fully functionalized furopyran moiety of azadirachtins.; SCI(E); PubMed; 0; ARTICLE; gongjx@pku.edu.cn; tuopingluo@pku.edu.cn; zyang@pku.edu.cn
语种	英语
内容类型	期刊论文
源URL	[http://ir.pku.edu.cn/handle/20.500.11897/188008]
专题	化学与分子工程学院生命科学学院
推荐引用方式 GB/T 7714	Tan Ceheng,Chen Wei,Mu Xinpeng,et al. Synthetic Progress toward Azadirachtins. 2. Enantio- and Diastereoselective Synthesis of the Right-Wing Fragment of 11-epi-Azadirachtin I[J]. organic letters,2015.
APA	Tan Ceheng.,Chen Wei.,Mu Xinpeng.,Chen Qi.,Gong Jianxian.,...&Yang Zhen.(2015).Synthetic Progress toward Azadirachtins. 2. Enantio- and Diastereoselective Synthesis of the Right-Wing Fragment of 11-epi-Azadirachtin I.organic letters.
MLA	Tan Ceheng,et al."Synthetic Progress toward Azadirachtins. 2. Enantio- and Diastereoselective Synthesis of the Right-Wing Fragment of 11-epi-Azadirachtin I".organic letters (2015).