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Li R, Zhao Y, Wang H, et al. Selective synthesis of formamides, 1,2-bis(N-heterocyclic)ethanes and methylamines from cyclic amines and CO. Chem Sci. 2019;10(42):9822-9828doi: 10.1039/c9sc03242h.
Li, R., Zhao, Y., Wang, H., Xiang, J., Wu, Y., Yu, B., Han, B., & Liu, Z. (2019). Selective synthesis of formamides, 1,2-bis(N-heterocyclic)ethanes and methylamines from cyclic amines and CO. Chemical science, 10(42), 9822-9828. https://doi.org/10.1039/c9sc03242h
Li, Ruipeng, et al. "Selective synthesis of formamides, 1,2-bis(N-heterocyclic)ethanes and methylamines from cyclic amines and CO." Chemical science vol. 10,42 (2019): 9822-9828. doi: https://doi.org/10.1039/c9sc03242h
Li R, Zhao Y, Wang H, Xiang J, Wu Y, Yu B, Han B, Liu Z. Selective synthesis of formamides, 1,2-bis(N-heterocyclic)ethanes and methylamines from cyclic amines and CO. Chem Sci. 2019 Sep 03;10(42):9822-9828. doi: 10.1039/c9sc03242h. eCollection 2019 Nov 14. PMID: 32015804; PMCID: PMC6977556.
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Chem Sci. 2019 Sep 03;10(42):9822-9828. doi: 10.1039/c9sc03242h. eCollection 2019 Nov 14.

Selective synthesis of formamides, 1,2-bis(N-heterocyclic)ethanes and methylamines from cyclic amines and CO.

Chemical science

Ruipeng Li, Yanfei Zhao, Huan Wang, Junfeng Xiang, Yunyan Wu, Bo Yu, Buxing Han, Zhimin Liu

Affiliations

  1. Beijing National Laboratory for Molecular Sciences , Key Laboratory of Colloid, Interface and Thermodynamics , CAS Research , Institute of Chemistry , Chinese Academy of Sciences , Beijing 100190 , China . Email: [email protected] ; Email: [email protected].
  2. University of Chinese Academy of Sciences , Beijing 100049 , China.
  3. Physical Science Laboratory , Huairou National Comprehensive Science Center , China.

PMID: 32015804 PMCID: PMC6977556 DOI: 10.1039/c9sc03242h

Abstract

The reduction of CO

This journal is © The Royal Society of Chemistry 2019.

References

  1. Nat Commun. 2018 Aug 27;9(1):3457 - PubMed
  2. J Am Chem Soc. 2016 Nov 2;138(43):14198-14201 - PubMed
  3. Chem Sci. 2015 Apr 1;6(4):2297-2301 - PubMed
  4. Chemistry. 2014 May 19;20(21):6264-7 - PubMed
  5. Chem Rev. 2017 May 24;117(10):6834-6880 - PubMed
  6. Angew Chem Int Ed Engl. 2013 Sep 9;52(37):9620-33 - PubMed
  7. Angew Chem Int Ed Engl. 2017 Jun 6;56(24):6843-6847 - PubMed
  8. J Am Chem Soc. 2012 Feb 15;134(6):2934-7 - PubMed
  9. Inorg Chem. 2017 Jun 19;56(12):7301-7305 - PubMed
  10. Chem Commun (Camb). 2016 May 5;52(39):6545-8 - PubMed
  11. Nat Commun. 2017 Aug 2;8(1):175 - PubMed
  12. Sci Adv. 2018 Oct 05;4(10):eaas9319 - PubMed
  13. J Org Chem. 2006 Dec 22;71(26):9873-6 - PubMed
  14. ChemSusChem. 2015 Oct 26;8(20):3489-96 - PubMed
  15. Chem Sci. 2019 Feb 11;10(11):3161-3167 - PubMed
  16. Angew Chem Int Ed Engl. 2014 Oct 6;53(41):11010-4 - PubMed
  17. Nat Commun. 2016 Dec 16;7:13782 - PubMed
  18. J Am Chem Soc. 2015 Oct 28;137(42):13580-7 - PubMed
  19. Chem Commun (Camb). 2002 Aug 7;(15):1612-3 - PubMed

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