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The highly enantioselective addition of indoles and pyrroles to isatins-derived N-Boc ketimines catalyzed by chiral phosphoric acids.
Chem Commun (Camb). 2012 Aug 18; 48(64):8003-5.CC

Abstract

The first asymmetric aza-Friedel-Crafts reaction of indoles and pyrroles with isatin-derived N-Boc ketimines catalyzed by chiral phosphoric acids is reported. In general, derivatives of substituted 3-amino-2-oxindoles were obtained with excellent enantioselectivities and high yields.

Authors+Show Affiliations

Key Laboratory of Preclinical Study for New Drugs of Gansu Province, School of Basic Medical Sciences, Lanzhou University, Lanzhou, 730000, China.No affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

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

Language

eng

PubMed ID

22773055

Citation

Feng, Jingchao, et al. "The Highly Enantioselective Addition of Indoles and Pyrroles to Isatins-derived N-Boc Ketimines Catalyzed By Chiral Phosphoric Acids." Chemical Communications (Cambridge, England), vol. 48, no. 64, 2012, pp. 8003-5.
Feng J, Yan W, Wang D, et al. The highly enantioselective addition of indoles and pyrroles to isatins-derived N-Boc ketimines catalyzed by chiral phosphoric acids. Chem Commun (Camb). 2012;48(64):8003-5.
Feng, J., Yan, W., Wang, D., Li, P., Sun, Q., & Wang, R. (2012). The highly enantioselective addition of indoles and pyrroles to isatins-derived N-Boc ketimines catalyzed by chiral phosphoric acids. Chemical Communications (Cambridge, England), 48(64), 8003-5. https://doi.org/10.1039/c2cc33200k
Feng J, et al. The Highly Enantioselective Addition of Indoles and Pyrroles to Isatins-derived N-Boc Ketimines Catalyzed By Chiral Phosphoric Acids. Chem Commun (Camb). 2012 Aug 18;48(64):8003-5. PubMed PMID: 22773055.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - The highly enantioselective addition of indoles and pyrroles to isatins-derived N-Boc ketimines catalyzed by chiral phosphoric acids. AU - Feng,Jingchao, AU - Yan,Wenjin, AU - Wang,Dong, AU - Li,Peng, AU - Sun,Quantao, AU - Wang,Rui, Y1 - 2012/07/06/ PY - 2012/7/10/entrez PY - 2012/7/10/pubmed PY - 2012/11/13/medline SP - 8003 EP - 5 JF - Chemical communications (Cambridge, England) JO - Chem Commun (Camb) VL - 48 IS - 64 N2 - The first asymmetric aza-Friedel-Crafts reaction of indoles and pyrroles with isatin-derived N-Boc ketimines catalyzed by chiral phosphoric acids is reported. In general, derivatives of substituted 3-amino-2-oxindoles were obtained with excellent enantioselectivities and high yields. SN - 1364-548X UR - https://www.unboundmedicine.com/medline/citation/22773055/The_highly_enantioselective_addition_of_indoles_and_pyrroles_to_isatins_derived_N_Boc_ketimines_catalyzed_by_chiral_phosphoric_acids_ L2 - https://doi.org/10.1039/c2cc33200k DB - PRIME DP - Unbound Medicine ER -