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Copper-catalyzed dimerization fragmentation cyclization reactions of (E)-1-en-4-yn-3-ols as a versatile approach for the synthesis of multisubstituted 1H-cyclopenta[b]naphthalenes.
Org Biomol Chem. 2011 Nov 07; 9(21):7461-7.OB

Abstract

An intermolecular condensation reaction of 1,3,5-triarylenynols catalyzed by copper is developed. This reaction is a straightforward method for the synthesis of highly conjugated 1H-cyclopenta[b]naphthalene. Fluorescent properties have been determined for some of the products.

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Publisher Full Text (DOI)

Authors+Show Affiliations

Wang XC
State Key Laboratory of Applied Organic Chemistry, Lanzhou University, Lanzhou, 730000, P. R. China.
Hu J
No affiliation info available
Sun PS
No affiliation info available
Zhong MJ
No affiliation info available
Ali S
No affiliation info available
Liang YM
No affiliation info available

MeSH

AlkynesCatalysisCopperCyclizationCyclopentanesMolecular StructureNaphthalenesOrganometallic CompoundsStereoisomerism

Pub Type(s)

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

Language

eng

PubMed ID

21915418

Citation

Wang, Xiang-Chuan, et al. "Copper-catalyzed Dimerization Fragmentation Cyclization Reactions of (E)-1-en-4-yn-3-ols as a Versatile Approach for the Synthesis of Multisubstituted 1H-cyclopenta[b]naphthalenes." Organic & Biomolecular Chemistry, vol. 9, no. 21, 2011, pp. 7461-7.
Wang XC, Hu J, Sun PS, et al. Copper-catalyzed dimerization fragmentation cyclization reactions of (E)-1-en-4-yn-3-ols as a versatile approach for the synthesis of multisubstituted 1H-cyclopenta[b]naphthalenes. Org Biomol Chem. 2011;9(21):7461-7.
Wang, X. C., Hu, J., Sun, P. S., Zhong, M. J., Ali, S., & Liang, Y. M. (2011). Copper-catalyzed dimerization fragmentation cyclization reactions of (E)-1-en-4-yn-3-ols as a versatile approach for the synthesis of multisubstituted 1H-cyclopenta[b]naphthalenes. Organic & Biomolecular Chemistry, 9(21), 7461-7. https://doi.org/10.1039/c1ob06087b
Wang XC, et al. Copper-catalyzed Dimerization Fragmentation Cyclization Reactions of (E)-1-en-4-yn-3-ols as a Versatile Approach for the Synthesis of Multisubstituted 1H-cyclopenta[b]naphthalenes. Org Biomol Chem. 2011 Nov 7;9(21):7461-7. PubMed PMID: 21915418.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Copper-catalyzed dimerization fragmentation cyclization reactions of (E)-1-en-4-yn-3-ols as a versatile approach for the synthesis of multisubstituted 1H-cyclopenta[b]naphthalenes. AU - Wang,Xiang-Chuan, AU - Hu,Jie, AU - Sun,Peng-Shuai, AU - Zhong,Mei-Jin, AU - Ali,Shaukat, AU - Liang,Yong-Min, Y1 - 2011/09/14/ PY - 2011/9/15/entrez PY - 2011/9/15/pubmed PY - 2012/2/4/medline SP - 7461 EP - 7 JF - Organic & biomolecular chemistry JO - Org Biomol Chem VL - 9 IS - 21 N2 - An intermolecular condensation reaction of 1,3,5-triarylenynols catalyzed by copper is developed. This reaction is a straightforward method for the synthesis of highly conjugated 1H-cyclopenta[b]naphthalene. Fluorescent properties have been determined for some of the products. SN - 1477-0539 UR - https://www.unboundmedicine.com/medline/citation/21915418/Copper_catalyzed_dimerization_fragmentation_cyclization_reactions_of__E__1_en_4_yn_3_ols_as_a_versatile_approach_for_the_synthesis_of_multisubstituted_1H_cyclopenta[b]naphthalenes_ L2 - https://doi.org/10.1039/c1ob06087b DB - PRIME DP - Unbound Medicine ER -