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Enantioselective modular synthesis of 2,4-disubstituted cyclopentenones by iridium-catalyzed allylic alkylation.
Angew Chem Int Ed Engl. 2006 Apr 03; 45(15):2466-9.AC

Authors+Show Affiliations

Organisch-Chemisches Institut der Universität Heidelberg, Im Neuenheimer Feld 270, 69120 Heidelberg, Germany.No affiliation info availableNo affiliation info available

Pub Type(s)

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

Language

eng

PubMed ID

16526068

Citation

Schelwies, Mathias, et al. "Enantioselective Modular Synthesis of 2,4-disubstituted Cyclopentenones By Iridium-catalyzed Allylic Alkylation." Angewandte Chemie (International Ed. in English), vol. 45, no. 15, 2006, pp. 2466-9.
Schelwies M, Dübon P, Helmchen G. Enantioselective modular synthesis of 2,4-disubstituted cyclopentenones by iridium-catalyzed allylic alkylation. Angew Chem Int Ed Engl. 2006;45(15):2466-9.
Schelwies, M., Dübon, P., & Helmchen, G. (2006). Enantioselective modular synthesis of 2,4-disubstituted cyclopentenones by iridium-catalyzed allylic alkylation. Angewandte Chemie (International Ed. in English), 45(15), 2466-9.
Schelwies M, Dübon P, Helmchen G. Enantioselective Modular Synthesis of 2,4-disubstituted Cyclopentenones By Iridium-catalyzed Allylic Alkylation. Angew Chem Int Ed Engl. 2006 Apr 3;45(15):2466-9. PubMed PMID: 16526068.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Enantioselective modular synthesis of 2,4-disubstituted cyclopentenones by iridium-catalyzed allylic alkylation. AU - Schelwies,Mathias, AU - Dübon,Pierre, AU - Helmchen,Günter, PY - 2006/3/10/pubmed PY - 2007/5/23/medline PY - 2006/3/10/entrez SP - 2466 EP - 9 JF - Angewandte Chemie (International ed. in English) JO - Angew Chem Int Ed Engl VL - 45 IS - 15 SN - 1433-7851 UR - https://www.unboundmedicine.com/medline/citation/16526068/Enantioselective_modular_synthesis_of_24_disubstituted_cyclopentenones_by_iridium_catalyzed_allylic_alkylation_ DB - PRIME DP - Unbound Medicine ER -