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Mild rhodium(III)-catalyzed cyclization of amides with α,β-unsaturated aldehydes and ketones to azepinones: application to the synthesis of the homoprotoberberine framework.
Angew Chem Int Ed Engl. 2013 May 10; 52(20):5393-7.AC

Authors+Show Affiliations

Universität Münster, Organisch-Chemisches Institut, Corrensstrasse 40, 48149 Münster, Germany.No affiliation info availableNo affiliation info available

Pub Type(s)

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

Language

eng

PubMed ID

23592552

Citation

Shi, Zhuangzhi, et al. "Mild rhodium(III)-catalyzed Cyclization of Amides With Α,β-unsaturated Aldehydes and Ketones to Azepinones: Application to the Synthesis of the Homoprotoberberine Framework." Angewandte Chemie (International Ed. in English), vol. 52, no. 20, 2013, pp. 5393-7.
Shi Z, Grohmann C, Glorius F. Mild rhodium(III)-catalyzed cyclization of amides with α,β-unsaturated aldehydes and ketones to azepinones: application to the synthesis of the homoprotoberberine framework. Angew Chem Int Ed Engl. 2013;52(20):5393-7.
Shi, Z., Grohmann, C., & Glorius, F. (2013). Mild rhodium(III)-catalyzed cyclization of amides with α,β-unsaturated aldehydes and ketones to azepinones: application to the synthesis of the homoprotoberberine framework. Angewandte Chemie (International Ed. in English), 52(20), 5393-7. https://doi.org/10.1002/anie.201301426
Shi Z, Grohmann C, Glorius F. Mild rhodium(III)-catalyzed Cyclization of Amides With Α,β-unsaturated Aldehydes and Ketones to Azepinones: Application to the Synthesis of the Homoprotoberberine Framework. Angew Chem Int Ed Engl. 2013 May 10;52(20):5393-7. PubMed PMID: 23592552.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Mild rhodium(III)-catalyzed cyclization of amides with α,β-unsaturated aldehydes and ketones to azepinones: application to the synthesis of the homoprotoberberine framework. AU - Shi,Zhuangzhi, AU - Grohmann,Christoph, AU - Glorius,Frank, Y1 - 2013/04/16/ PY - 2013/02/18/received PY - 2013/4/18/entrez PY - 2013/4/18/pubmed PY - 2013/11/1/medline SP - 5393 EP - 7 JF - Angewandte Chemie (International ed. in English) JO - Angew Chem Int Ed Engl VL - 52 IS - 20 SN - 1521-3773 UR - https://www.unboundmedicine.com/medline/citation/23592552/Mild_rhodium_III__catalyzed_cyclization_of_amides_with_αβ_unsaturated_aldehydes_and_ketones_to_azepinones:_application_to_the_synthesis_of_the_homoprotoberberine_framework_ L2 - https://doi.org/10.1002/anie.201301426 DB - PRIME DP - Unbound Medicine ER -