New insight into Ni(II)-catalyzed cyclization reactions of propargylic compounds with soft nucleophiles: novel indenes formation.J Org Chem. 2008 May 16; 73(10):3837-41.JO
Abstract
We have disclosed a very nice advance of nickel(II)-catalyzed carboannulation reactions. Highly substituted indene derivatives are readily prepared in moderate to excellent yields under very mild reaction conditions in air via a nickel(II)-catalyzed cyclization of propargylic compounds with soft nucleophiles.
Links
Pub Type(s)
Journal Article
Language
eng
PubMed ID
18410142
Citation
Gou, Fa-Rong, et al. "New Insight Into Ni(II)-catalyzed Cyclization Reactions of Propargylic Compounds With Soft Nucleophiles: Novel Indenes Formation." The Journal of Organic Chemistry, vol. 73, no. 10, 2008, pp. 3837-41.
Gou FR, Bi HP, Guo LN, et al. New insight into Ni(II)-catalyzed cyclization reactions of propargylic compounds with soft nucleophiles: novel indenes formation. J Org Chem. 2008;73(10):3837-41.
Gou, F. R., Bi, H. P., Guo, L. N., Guan, Z. H., Liu, X. Y., & Liang, Y. M. (2008). New insight into Ni(II)-catalyzed cyclization reactions of propargylic compounds with soft nucleophiles: novel indenes formation. The Journal of Organic Chemistry, 73(10), 3837-41. https://doi.org/10.1021/jo800155a
Gou FR, et al. New Insight Into Ni(II)-catalyzed Cyclization Reactions of Propargylic Compounds With Soft Nucleophiles: Novel Indenes Formation. J Org Chem. 2008 May 16;73(10):3837-41. PubMed PMID: 18410142.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR
T1 - New insight into Ni(II)-catalyzed cyclization reactions of propargylic compounds with soft nucleophiles: novel indenes formation.
AU - Gou,Fa-Rong,
AU - Bi,Hai-Peng,
AU - Guo,Li-Na,
AU - Guan,Zheng-Hui,
AU - Liu,Xue-Yuan,
AU - Liang,Yong-Min,
Y1 - 2008/04/15/
PY - 2008/4/16/pubmed
PY - 2008/8/14/medline
PY - 2008/4/16/entrez
SP - 3837
EP - 41
JF - The Journal of organic chemistry
JO - J Org Chem
VL - 73
IS - 10
N2 - We have disclosed a very nice advance of nickel(II)-catalyzed carboannulation reactions. Highly substituted indene derivatives are readily prepared in moderate to excellent yields under very mild reaction conditions in air via a nickel(II)-catalyzed cyclization of propargylic compounds with soft nucleophiles.
SN - 0022-3263
UR - https://www.unboundmedicine.com/medline/citation/18410142/New_insight_into_Ni_II__catalyzed_cyclization_reactions_of_propargylic_compounds_with_soft_nucleophiles:_novel_indenes_formation_
DB - PRIME
DP - Unbound Medicine
ER -