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Access to indenones by rhodium(III)-catalyzed C-H annulation of arylnitrones with internal alkynes.
Org Lett. 2013 Nov 01; 15(21):5440-3.OL

Abstract

Under redox-neutral conditions, rhodium(III)-catalyzed C-H annulation of N-tert-butyl-α-arylnitrones with internal alkynes has been realized for the synthesis of indenones under mild conditions. This reaction proceeded in moderate to high yields and with good functional group tolerance.

Authors+Show Affiliations

Dalian Institute of Chemical Physics, Chinese Academy of Sciences , Dalian 116023, China , and State Key Laboratory of Fine Chemicals, Dalian University of Technology , Dalian 116024, China.No affiliation info availableNo affiliation info available

Pub Type(s)

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

Language

eng

PubMed ID

24117207

Citation

Qi, Zisong, et al. "Access to Indenones By rhodium(III)-catalyzed C-H Annulation of Arylnitrones With Internal Alkynes." Organic Letters, vol. 15, no. 21, 2013, pp. 5440-3.
Qi Z, Wang M, Li X. Access to indenones by rhodium(III)-catalyzed C-H annulation of arylnitrones with internal alkynes. Org Lett. 2013;15(21):5440-3.
Qi, Z., Wang, M., & Li, X. (2013). Access to indenones by rhodium(III)-catalyzed C-H annulation of arylnitrones with internal alkynes. Organic Letters, 15(21), 5440-3. https://doi.org/10.1021/ol4025309
Qi Z, Wang M, Li X. Access to Indenones By rhodium(III)-catalyzed C-H Annulation of Arylnitrones With Internal Alkynes. Org Lett. 2013 Nov 1;15(21):5440-3. PubMed PMID: 24117207.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Access to indenones by rhodium(III)-catalyzed C-H annulation of arylnitrones with internal alkynes. AU - Qi,Zisong, AU - Wang,Mei, AU - Li,Xingwei, Y1 - 2013/10/11/ PY - 2013/10/15/entrez PY - 2013/10/15/pubmed PY - 2014/4/29/medline SP - 5440 EP - 3 JF - Organic letters JO - Org Lett VL - 15 IS - 21 N2 - Under redox-neutral conditions, rhodium(III)-catalyzed C-H annulation of N-tert-butyl-α-arylnitrones with internal alkynes has been realized for the synthesis of indenones under mild conditions. This reaction proceeded in moderate to high yields and with good functional group tolerance. SN - 1523-7052 UR - https://www.unboundmedicine.com/medline/citation/24117207/Access_to_indenones_by_rhodium_III__catalyzed_C_H_annulation_of_arylnitrones_with_internal_alkynes_ L2 - https://doi.org/10.1021/ol4025309 DB - PRIME DP - Unbound Medicine ER -