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Synthesis of substituted naphthalenes by the palladium-catalyzed annulation of internal alkynes.
Org Lett. 2002 Jul 25; 4(15):2505-8.OL

Abstract

[reaction: see text] A variety of substituted naphthalenes have been prepared by the palladium-catalyzed carboannulation of internal alkynes. This method (1) forms two new carbon-carbon bonds in a single step, (2) accommodates a variety of functional groups, and (3) affords excellent yields of highly substituted naphthalenes.

Authors+Show Affiliations

Huang Q
Department of Chemistry, Iowa State University, Ames, Iowa 50011, USA.
Larock RC
No affiliation info available

MeSH

AlkynesCatalysisChemistry, PharmaceuticalCyclizationNaphthalenesPalladium

Pub Type(s)

Journal Article
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

12123362

Citation

Huang, Qinhua, and Richard C. Larock. "Synthesis of Substituted Naphthalenes By the Palladium-catalyzed Annulation of Internal Alkynes." Organic Letters, vol. 4, no. 15, 2002, pp. 2505-8.
Huang Q, Larock RC. Synthesis of substituted naphthalenes by the palladium-catalyzed annulation of internal alkynes. Org Lett. 2002;4(15):2505-8.
Huang, Q., & Larock, R. C. (2002). Synthesis of substituted naphthalenes by the palladium-catalyzed annulation of internal alkynes. Organic Letters, 4(15), 2505-8.
Huang Q, Larock RC. Synthesis of Substituted Naphthalenes By the Palladium-catalyzed Annulation of Internal Alkynes. Org Lett. 2002 Jul 25;4(15):2505-8. PubMed PMID: 12123362.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Synthesis of substituted naphthalenes by the palladium-catalyzed annulation of internal alkynes. AU - Huang,Qinhua, AU - Larock,Richard C, PY - 2002/7/19/pubmed PY - 2003/8/2/medline PY - 2002/7/19/entrez SP - 2505 EP - 8 JF - Organic letters JO - Org Lett VL - 4 IS - 15 N2 - [reaction: see text] A variety of substituted naphthalenes have been prepared by the palladium-catalyzed carboannulation of internal alkynes. This method (1) forms two new carbon-carbon bonds in a single step, (2) accommodates a variety of functional groups, and (3) affords excellent yields of highly substituted naphthalenes. SN - 1523-7060 UR - https://www.unboundmedicine.com/medline/citation/12123362/Synthesis_of_substituted_naphthalenes_by_the_palladium_catalyzed_annulation_of_internal_alkynes_ DB - PRIME DP - Unbound Medicine ER -