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Rhodium(III)-catalyzed C-H alkynylation of azomethine ylides under mild conditions.
Org Biomol Chem. 2014 Dec 14; 12(46):9329-32.OB

Abstract

Rh(III)-catalyzed efficient C-H alkynylation of azomethine imines with alkynylated hypervalent iodine is developed under mild conditions. A broad scope of azomethine imines and alkyne substrates is established. The azomethine acts as a masked aldehyde and circumvents its poor directing effect.

Authors+Show Affiliations

School of Chemistry and Pharmaceutical Engineering, Qilu University of Technology, Ji'nan 250353, China.No affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

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

Language

eng

PubMed ID

25325793

Citation

Zhang, Xueyun, et al. "Rhodium(III)-catalyzed C-H Alkynylation of Azomethine Ylides Under Mild Conditions." Organic & Biomolecular Chemistry, vol. 12, no. 46, 2014, pp. 9329-32.
Zhang X, Qi Z, Gao J, et al. Rhodium(III)-catalyzed C-H alkynylation of azomethine ylides under mild conditions. Org Biomol Chem. 2014;12(46):9329-32.
Zhang, X., Qi, Z., Gao, J., & Li, X. (2014). Rhodium(III)-catalyzed C-H alkynylation of azomethine ylides under mild conditions. Organic & Biomolecular Chemistry, 12(46), 9329-32. https://doi.org/10.1039/c4ob01596g
Zhang X, et al. Rhodium(III)-catalyzed C-H Alkynylation of Azomethine Ylides Under Mild Conditions. Org Biomol Chem. 2014 Dec 14;12(46):9329-32. PubMed PMID: 25325793.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Rhodium(III)-catalyzed C-H alkynylation of azomethine ylides under mild conditions. AU - Zhang,Xueyun, AU - Qi,Zisong, AU - Gao,Jian, AU - Li,Xingwei, Y1 - 2014/10/17/ PY - 2014/10/18/entrez PY - 2014/10/18/pubmed PY - 2015/6/30/medline SP - 9329 EP - 32 JF - Organic & biomolecular chemistry JO - Org Biomol Chem VL - 12 IS - 46 N2 - Rh(III)-catalyzed efficient C-H alkynylation of azomethine imines with alkynylated hypervalent iodine is developed under mild conditions. A broad scope of azomethine imines and alkyne substrates is established. The azomethine acts as a masked aldehyde and circumvents its poor directing effect. SN - 1477-0539 UR - https://www.unboundmedicine.com/medline/citation/25325793/Rhodium_III__catalyzed_C_H_alkynylation_of_azomethine_ylides_under_mild_conditions_ DB - PRIME DP - Unbound Medicine ER -