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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.

Authors+Show Affiliations

State Key Laboratory of Applied Organic Chemistry, Lanzhou University, and State Key Laboratory of Solid Lubrication, Lanzhou Institute of Chemical Physics, Chinese Academy of Science, Lanzhou, PR China.No affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

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 -