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Ruthenium-catalyzed intramolecular allylic dearomatization reaction of indole derivatives.
Org Lett. 2013 Jul 19; 15(14):3746-9.OL

Abstract

An efficient synthesis of spiroindolenine derivatives via a ruthenium-catalyzed intramolecular allylic dearomatization reaction has been developed. This method features a wide substrate scope, mild reaction conditions, and an operationally simple procedure.

Authors+Show Affiliations

State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Lu, Shanghai 200032, China.No 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

23841581

Citation

Zhang, Xiao, et al. "Ruthenium-catalyzed Intramolecular Allylic Dearomatization Reaction of Indole Derivatives." Organic Letters, vol. 15, no. 14, 2013, pp. 3746-9.
Zhang X, Liu WB, Wu QF, et al. Ruthenium-catalyzed intramolecular allylic dearomatization reaction of indole derivatives. Org Lett. 2013;15(14):3746-9.
Zhang, X., Liu, W. B., Wu, Q. F., & You, S. L. (2013). Ruthenium-catalyzed intramolecular allylic dearomatization reaction of indole derivatives. Organic Letters, 15(14), 3746-9. https://doi.org/10.1021/ol4016578
Zhang X, et al. Ruthenium-catalyzed Intramolecular Allylic Dearomatization Reaction of Indole Derivatives. Org Lett. 2013 Jul 19;15(14):3746-9. PubMed PMID: 23841581.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Ruthenium-catalyzed intramolecular allylic dearomatization reaction of indole derivatives. AU - Zhang,Xiao, AU - Liu,Wen-Bo, AU - Wu,Qing-Feng, AU - You,Shu-Li, Y1 - 2013/07/10/ PY - 2013/7/12/entrez PY - 2013/7/12/pubmed PY - 2014/2/4/medline SP - 3746 EP - 9 JF - Organic letters JO - Org Lett VL - 15 IS - 14 N2 - An efficient synthesis of spiroindolenine derivatives via a ruthenium-catalyzed intramolecular allylic dearomatization reaction has been developed. This method features a wide substrate scope, mild reaction conditions, and an operationally simple procedure. SN - 1523-7052 UR - https://www.unboundmedicine.com/medline/citation/23841581/Ruthenium_catalyzed_intramolecular_allylic_dearomatization_reaction_of_indole_derivatives_ L2 - https://doi.org/10.1021/ol4016578 DB - PRIME DP - Unbound Medicine ER -