Synthesis of N-alkoxycarbonyl ketimines derived from isatins and their application in enantioselective synthesis of 3-aminooxindoles.Org Lett. 2012 May 18; 14(10):2512-5.OL
Abstract
A simple and general method in the synthesis of N-alkoxycarbonyl ketimines derived from isatins has been described first. Generally, the enantioselective addition of 1,3-dicarbonyl compounds to this kind of ketimine affords chiral 3-amino oxindoles in high yield and excellent ee.
Links
Pub Type(s)
Journal Article
Research Support, Non-U.S. Gov't
Language
eng
PubMed ID
22540839
Citation
Yan, Wenjin, et al. "Synthesis of N-alkoxycarbonyl Ketimines Derived From Isatins and Their Application in Enantioselective Synthesis of 3-aminooxindoles." Organic Letters, vol. 14, no. 10, 2012, pp. 2512-5.
Yan W, Wang D, Feng J, et al. Synthesis of N-alkoxycarbonyl ketimines derived from isatins and their application in enantioselective synthesis of 3-aminooxindoles. Org Lett. 2012;14(10):2512-5.
Yan, W., Wang, D., Feng, J., Li, P., Zhao, D., & Wang, R. (2012). Synthesis of N-alkoxycarbonyl ketimines derived from isatins and their application in enantioselective synthesis of 3-aminooxindoles. Organic Letters, 14(10), 2512-5. https://doi.org/10.1021/ol3007953
Yan W, et al. Synthesis of N-alkoxycarbonyl Ketimines Derived From Isatins and Their Application in Enantioselective Synthesis of 3-aminooxindoles. Org Lett. 2012 May 18;14(10):2512-5. PubMed PMID: 22540839.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR
T1 - Synthesis of N-alkoxycarbonyl ketimines derived from isatins and their application in enantioselective synthesis of 3-aminooxindoles.
AU - Yan,Wenjin,
AU - Wang,Dong,
AU - Feng,Jingchao,
AU - Li,Peng,
AU - Zhao,Depeng,
AU - Wang,Rui,
Y1 - 2012/04/27/
PY - 2012/5/1/entrez
PY - 2012/5/1/pubmed
PY - 2014/4/26/medline
SP - 2512
EP - 5
JF - Organic letters
JO - Org Lett
VL - 14
IS - 10
N2 - A simple and general method in the synthesis of N-alkoxycarbonyl ketimines derived from isatins has been described first. Generally, the enantioselective addition of 1,3-dicarbonyl compounds to this kind of ketimine affords chiral 3-amino oxindoles in high yield and excellent ee.
SN - 1523-7052
UR - https://www.unboundmedicine.com/medline/citation/22540839/Synthesis_of_N_alkoxycarbonyl_ketimines_derived_from_isatins_and_their_application_in_enantioselective_synthesis_of_3_aminooxindoles_
L2 - https://doi.org/10.1021/ol3007953
DB - PRIME
DP - Unbound Medicine
ER -