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Construction of polycyclic spiro-indolines via an intramolecular oxidative coupling/cyclization cascade reaction process.
Org Lett. 2012 Mar 16; 14(6):1405-7.OL

Abstract

An efficient protocol for assembling a polycyclic spiroindoline scaffold is developed, which involves an intramolecular oxidative coupling of dianions derived from indole-embodied β-ketoamides using iodine as the oxidant, and subsequent attack of oxygen anion to the resultant imine moiety. A number of tetracyclic spiroindolines are prepared with moderate to good yields.

Authors+Show Affiliations

School of Pharmacy, East China University of Science and Technology, 130 Meilong Road, Shanghai 200237, China.No affiliation info availableNo affiliation info available

Pub Type(s)

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

Language

eng

PubMed ID

22400980

Citation

Fan, Feng, et al. "Construction of Polycyclic Spiro-indolines Via an Intramolecular Oxidative Coupling/cyclization Cascade Reaction Process." Organic Letters, vol. 14, no. 6, 2012, pp. 1405-7.
Fan F, Xie W, Ma D. Construction of polycyclic spiro-indolines via an intramolecular oxidative coupling/cyclization cascade reaction process. Org Lett. 2012;14(6):1405-7.
Fan, F., Xie, W., & Ma, D. (2012). Construction of polycyclic spiro-indolines via an intramolecular oxidative coupling/cyclization cascade reaction process. Organic Letters, 14(6), 1405-7. https://doi.org/10.1021/ol3003496
Fan F, Xie W, Ma D. Construction of Polycyclic Spiro-indolines Via an Intramolecular Oxidative Coupling/cyclization Cascade Reaction Process. Org Lett. 2012 Mar 16;14(6):1405-7. PubMed PMID: 22400980.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Construction of polycyclic spiro-indolines via an intramolecular oxidative coupling/cyclization cascade reaction process. AU - Fan,Feng, AU - Xie,Weiqing, AU - Ma,Dawei, Y1 - 2012/03/08/ PY - 2012/3/10/entrez PY - 2012/3/10/pubmed PY - 2012/6/13/medline SP - 1405 EP - 7 JF - Organic letters JO - Org Lett VL - 14 IS - 6 N2 - An efficient protocol for assembling a polycyclic spiroindoline scaffold is developed, which involves an intramolecular oxidative coupling of dianions derived from indole-embodied β-ketoamides using iodine as the oxidant, and subsequent attack of oxygen anion to the resultant imine moiety. A number of tetracyclic spiroindolines are prepared with moderate to good yields. SN - 1523-7052 UR - https://www.unboundmedicine.com/medline/citation/22400980/Construction_of_polycyclic_spiro_indolines_via_an_intramolecular_oxidative_coupling/cyclization_cascade_reaction_process_ L2 - https://doi.org/10.1021/ol3003496 DB - PRIME DP - Unbound Medicine ER -