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Rhodium-catalyzed cycloisomerization: formation of indoles, benzofurans, and enol lactones.
Angew Chem Int Ed Engl. 2007; 46(12):2074-7.AC

Authors+Show Affiliations

Department of Chemistry, Stanford University, Stanford, CA 94305-5080, USA. bmtrost@stanford.eduNo affiliation info available

Pub Type(s)

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

Language

eng

PubMed ID

17285670

Citation

Trost, Barry M., and Andrew McClory. "Rhodium-catalyzed Cycloisomerization: Formation of Indoles, Benzofurans, and Enol Lactones." Angewandte Chemie (International Ed. in English), vol. 46, no. 12, 2007, pp. 2074-7.
Trost BM, McClory A. Rhodium-catalyzed cycloisomerization: formation of indoles, benzofurans, and enol lactones. Angew Chem Int Ed Engl. 2007;46(12):2074-7.
Trost, B. M., & McClory, A. (2007). Rhodium-catalyzed cycloisomerization: formation of indoles, benzofurans, and enol lactones. Angewandte Chemie (International Ed. in English), 46(12), 2074-7.
Trost BM, McClory A. Rhodium-catalyzed Cycloisomerization: Formation of Indoles, Benzofurans, and Enol Lactones. Angew Chem Int Ed Engl. 2007;46(12):2074-7. PubMed PMID: 17285670.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Rhodium-catalyzed cycloisomerization: formation of indoles, benzofurans, and enol lactones. AU - Trost,Barry M, AU - McClory,Andrew, PY - 2007/2/8/pubmed PY - 2007/4/27/medline PY - 2007/2/8/entrez SP - 2074 EP - 7 JF - Angewandte Chemie (International ed. in English) JO - Angew Chem Int Ed Engl VL - 46 IS - 12 SN - 1433-7851 UR - https://www.unboundmedicine.com/medline/citation/17285670/Rhodium_catalyzed_cycloisomerization:_formation_of_indoles_benzofurans_and_enol_lactones_ L2 - https://doi.org/10.1002/anie.200604183 DB - PRIME DP - Unbound Medicine ER -