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Copper-catalyzed highly efficient multicomponent reactions: synthesis of 2-(sulfonylimino)-4-(alkylimino)azetidine derivatives.
Org Lett. 2007 Apr 12; 9(8):1585-7.OL

Abstract

[reaction: see text] Under very mild conditions, functionalized 2-(sulfonylimino)-4-(alkylimino)azetidine derivatives were prepared in good to excellent yields via a copper-catalyzed multicomponent reaction of readily available terminal alkynes, sulfonyl azides, and carbodiimides without the assistance of a base. The mechanism may be through a [2 + 2] cycloaddition.

Authors+Show Affiliations

College of Chemical Engineering and Materials Science and College of Pharmaceutical Science, Zhejiang University of Technology, Hangzhou 310014, People's Republic of China. xuxiaoliang@zjut.edu.cnNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article

Language

eng

PubMed ID

17381100

Citation

Xu, Xiaoliang, et al. "Copper-catalyzed Highly Efficient Multicomponent Reactions: Synthesis of 2-(sulfonylimino)-4-(alkylimino)azetidine Derivatives." Organic Letters, vol. 9, no. 8, 2007, pp. 1585-7.
Xu X, Cheng D, Li J, et al. Copper-catalyzed highly efficient multicomponent reactions: synthesis of 2-(sulfonylimino)-4-(alkylimino)azetidine derivatives. Org Lett. 2007;9(8):1585-7.
Xu, X., Cheng, D., Li, J., Guo, H., & Yan, J. (2007). Copper-catalyzed highly efficient multicomponent reactions: synthesis of 2-(sulfonylimino)-4-(alkylimino)azetidine derivatives. Organic Letters, 9(8), 1585-7.
Xu X, et al. Copper-catalyzed Highly Efficient Multicomponent Reactions: Synthesis of 2-(sulfonylimino)-4-(alkylimino)azetidine Derivatives. Org Lett. 2007 Apr 12;9(8):1585-7. PubMed PMID: 17381100.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Copper-catalyzed highly efficient multicomponent reactions: synthesis of 2-(sulfonylimino)-4-(alkylimino)azetidine derivatives. AU - Xu,Xiaoliang, AU - Cheng,Dongping, AU - Li,Jinghua, AU - Guo,Hongyun, AU - Yan,Jie, Y1 - 2007/03/24/ PY - 2007/3/27/pubmed PY - 2007/6/19/medline PY - 2007/3/27/entrez SP - 1585 EP - 7 JF - Organic letters JO - Org Lett VL - 9 IS - 8 N2 - [reaction: see text] Under very mild conditions, functionalized 2-(sulfonylimino)-4-(alkylimino)azetidine derivatives were prepared in good to excellent yields via a copper-catalyzed multicomponent reaction of readily available terminal alkynes, sulfonyl azides, and carbodiimides without the assistance of a base. The mechanism may be through a [2 + 2] cycloaddition. SN - 1523-7060 UR - https://www.unboundmedicine.com/medline/citation/17381100/Copper_catalyzed_highly_efficient_multicomponent_reactions:_synthesis_of_2__sulfonylimino__4__alkylimino_azetidine_derivatives_ L2 - https://doi.org/10.1021/ol070485x DB - PRIME DP - Unbound Medicine ER -