Pd(0)-catalyzed alkenylation and allylic dearomatization reactions between nucleophile-bearing indoles and propargyl carbonate.Org Lett. 2014 Aug 01; 16(15):3919-21.OL
Abstract
Spiroindolenine derivatives were synthesized by intermolecular Pd-catalyzed dearomatization of indoles. The reaction between nucleophile bearing indoles and propargyl carbonate proceeds in a cascade fashion providing spiroindolenines or spiroindolines in good to excellent yields.
Links
Pub Type(s)
Journal Article
Research Support, Non-U.S. Gov't
Language
eng
PubMed ID
24992703
Citation
Gao, Run-Duo, et al. "Pd(0)-catalyzed Alkenylation and Allylic Dearomatization Reactions Between Nucleophile-bearing Indoles and Propargyl Carbonate." Organic Letters, vol. 16, no. 15, 2014, pp. 3919-21.
Gao RD, Liu C, Dai LX, et al. Pd(0)-catalyzed alkenylation and allylic dearomatization reactions between nucleophile-bearing indoles and propargyl carbonate. Org Lett. 2014;16(15):3919-21.
Gao, R. D., Liu, C., Dai, L. X., Zhang, W., & You, S. L. (2014). Pd(0)-catalyzed alkenylation and allylic dearomatization reactions between nucleophile-bearing indoles and propargyl carbonate. Organic Letters, 16(15), 3919-21. https://doi.org/10.1021/ol501704q
Gao RD, et al. Pd(0)-catalyzed Alkenylation and Allylic Dearomatization Reactions Between Nucleophile-bearing Indoles and Propargyl Carbonate. Org Lett. 2014 Aug 1;16(15):3919-21. PubMed PMID: 24992703.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR
T1 - Pd(0)-catalyzed alkenylation and allylic dearomatization reactions between nucleophile-bearing indoles and propargyl carbonate.
AU - Gao,Run-Duo,
AU - Liu,Chuan,
AU - Dai,Li-Xin,
AU - Zhang,Wei,
AU - You,Shu-Li,
Y1 - 2014/07/03/
PY - 2014/7/4/entrez
PY - 2014/7/6/pubmed
PY - 2014/10/11/medline
SP - 3919
EP - 21
JF - Organic letters
JO - Org Lett
VL - 16
IS - 15
N2 - Spiroindolenine derivatives were synthesized by intermolecular Pd-catalyzed dearomatization of indoles. The reaction between nucleophile bearing indoles and propargyl carbonate proceeds in a cascade fashion providing spiroindolenines or spiroindolines in good to excellent yields.
SN - 1523-7052
UR - https://www.unboundmedicine.com/medline/citation/24992703/Pd_0__catalyzed_alkenylation_and_allylic_dearomatization_reactions_between_nucleophile_bearing_indoles_and_propargyl_carbonate_
DB - PRIME
DP - Unbound Medicine
ER -