Selective C-arylation of free (NH)-heteroarenes via catalytic C-H bond functionalization [J. Am. Chem. Soc. 2003, 125, 5274-5275]

No authors listed

No authors listed. J Am Chem Soc. 2006.

. 2006 Jun 28;128(25):8364.

doi: 10.1021/ja069965u.

No abstract available

Retraction of

Selective C-arylation of free (NH)-heteroarenes via catalytic C-H bond functionalization.
Sezen B, Sames D. Sezen B, et al. J Am Chem Soc. 2003 May 7;125(18):5274-5. doi: 10.1021/ja034848+. J Am Chem Soc. 2003. Retraction in: J Am Chem Soc. 2006 Jun 28;128(25):8364. doi: 10.1021/ja069965u. PMID: 12720429 Retracted.

Oxidative C-arylation of free (NH)-heterocycles via direct sp3 C-H bond functionalization [J. Am. Chem. Soc. 2004, 126, 13244-13246].
Sezen B, Sames D. Sezen B, et al. J Am Chem Soc. 2006 Mar 8;128(9):3102. doi: 10.1021/ja069957d. J Am Chem Soc. 2006. PMID: 16506793 No abstract available.
Selective C-arylation of free (NH)-heteroarenes via catalytic C-H bond functionalization.
Sezen B, Sames D. Sezen B, et al. J Am Chem Soc. 2003 May 7;125(18):5274-5. doi: 10.1021/ja034848+. J Am Chem Soc. 2003. Retraction in: J Am Chem Soc. 2006 Jun 28;128(25):8364. doi: 10.1021/ja069965u. PMID: 12720429 Retracted.
Selective and catalytic arylation of N-phenylpyrrolidine: (sp3) C-H bond functionalization in the absence of a directing group [J. Am. Chem. Soc. 2005, 127, 5284-5285].
Sezen B, Sames D. Sezen B, et al. J Am Chem Soc. 2006 Mar 8;128(9):3102. doi: 10.1021/ja0699586. J Am Chem Soc. 2006. PMID: 16506792 No abstract available.
Radical-driven peptide backbone dissociation tandem mass spectrometry.
Oh HB, Moon B. Oh HB, et al. Mass Spectrom Rev. 2015 Mar-Apr;34(2):116-32. doi: 10.1002/mas.21426. Epub 2014 May 26. Mass Spectrom Rev. 2015. PMID: 24863492 Review.
Recent advances in the transition metal-catalyzed twofold oxidative C-H bond activation strategy for C-C and C-N bond formation.
Cho SH, Kim JY, Kwak J, Chang S. Cho SH, et al. Chem Soc Rev. 2011 Oct;40(10):5068-83. doi: 10.1039/c1cs15082k. Epub 2011 Jun 6. Chem Soc Rev. 2011. PMID: 21643614 Review.