Tags

Type your tag names separated by a space and hit enter

Highly diastereo- and enantioselective [3+2] annulation of isatin-derived Morita-Baylis-Hillman carbonates with trifluoropyruvate catalyzed by tertiary amines.
Chem Commun (Camb). 2013 Dec 07; 49(94):11071-3.CC

Abstract

An enantioselective [3+2] annulation of Morita-Baylis-Hillman carbonates with trifluoropyruvate catalyzed by modified cinchona alkaloids was developed in good to excellent yields with excellent diastereo- and enantioselectivities.

Links

Publisher Full Text (DOI)

Authors+Show Affiliations

Zhong NJ
Beijing National Laboratory for Molecular Sciences (BNLMS), CAS Key Laboratory of Molecular Recognition and Function, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China. lliu@iccas.ac.cn.
Wei F
No affiliation info available
Xuan QQ
No affiliation info available
Liu L
No affiliation info available
Wang D
No affiliation info available
Chen YJ
No affiliation info available

MeSH

AminesCarbonatesCatalysisIsatinPyruvic AcidStereoisomerismSubstrate Specificity

Pub Type(s)

Journal Article
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

24141558

Citation

Zhong, Neng-Jun, et al. "Highly Diastereo- and Enantioselective [3+2] Annulation of Isatin-derived Morita-Baylis-Hillman Carbonates With Trifluoropyruvate Catalyzed By Tertiary Amines." Chemical Communications (Cambridge, England), vol. 49, no. 94, 2013, pp. 11071-3.
Zhong NJ, Wei F, Xuan QQ, et al. Highly diastereo- and enantioselective [3+2] annulation of isatin-derived Morita-Baylis-Hillman carbonates with trifluoropyruvate catalyzed by tertiary amines. Chem Commun (Camb). 2013;49(94):11071-3.
Zhong, N. J., Wei, F., Xuan, Q. Q., Liu, L., Wang, D., & Chen, Y. J. (2013). Highly diastereo- and enantioselective [3+2] annulation of isatin-derived Morita-Baylis-Hillman carbonates with trifluoropyruvate catalyzed by tertiary amines. Chemical Communications (Cambridge, England), 49(94), 11071-3. https://doi.org/10.1039/c3cc46490c
Zhong NJ, et al. Highly Diastereo- and Enantioselective [3+2] Annulation of Isatin-derived Morita-Baylis-Hillman Carbonates With Trifluoropyruvate Catalyzed By Tertiary Amines. Chem Commun (Camb). 2013 Dec 7;49(94):11071-3. PubMed PMID: 24141558.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Highly diastereo- and enantioselective [3+2] annulation of isatin-derived Morita-Baylis-Hillman carbonates with trifluoropyruvate catalyzed by tertiary amines. AU - Zhong,Neng-Jun, AU - Wei,Feng, AU - Xuan,Qing-Qing, AU - Liu,Li, AU - Wang,Dong, AU - Chen,Yong-Jun, PY - 2013/10/22/entrez PY - 2013/10/22/pubmed PY - 2014/6/3/medline SP - 11071 EP - 3 JF - Chemical communications (Cambridge, England) JO - Chem Commun (Camb) VL - 49 IS - 94 N2 - An enantioselective [3+2] annulation of Morita-Baylis-Hillman carbonates with trifluoropyruvate catalyzed by modified cinchona alkaloids was developed in good to excellent yields with excellent diastereo- and enantioselectivities. SN - 1364-548X UR - https://www.unboundmedicine.com/medline/citation/24141558/Highly_diastereo__and_enantioselective_[3+2]_annulation_of_isatin_derived_Morita_Baylis_Hillman_carbonates_with_trifluoropyruvate_catalyzed_by_tertiary_amines_ L2 - https://doi.org/10.1039/c3cc46490c DB - PRIME DP - Unbound Medicine ER -