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.
Links
MeSH
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 -