, Heterocycles in Natural Product Synthesis, vol.103, p.2285, 2003.
, Eur. J. Med. Chem, p.480, 2014.
, Expert Opin. Invest. Drugs, p.367, 2007.
, J. Heterocycl. Chem, vol.56, p.828, 1282.
, J. Heterocycl. Chem, p.1787, 1979.
, Chem. Sci, vol.6, pp.5128-5132, 2015.
, Chem. Sci, 2010.
, Acc. Chem. Res, p.3054, 1534.
, Chem. Soc. Rev, vol.43, p.40, 1926.
, Angew. Chem., Int. Ed, vol.55, p.11906, 2015.
, Angew. Chem., Int. Ed, vol.51, issue.4734, p.604, 2012.
, J. Am. Chem. Soc, vol.6, p.135, 1326.
Nevertheless N-centered radicals addition on alkynes have been already reported using classical radical initiator, J. Org. Chem, vol.47, issue.7011, p.813, 1413. ,
, Angew. Chem., Int. Ed, vol.53, p.3158, 2014.
, J. Org. Chem, p.10692, 2013.
, Chem. -Eur. J, 2013.
, Only one paper reported a radical ring closing of hydrazones on alkenes leading to pyrazolines without trapping of the radical initiator used, Org. Lett, p.3214, 2013.
, Angew. Chem., Int. Ed, p.12163, 2014.
, Chem. Soc. Rev, vol.57, p.2452, 1653.
, Chem. Commun, p.2442, 2012.
, Angew. Chem., Int. Ed, vol.135, p.2487, 2013.
, The photo-induced Smiles rearrangement has been recently reported exclusively on di?uorobromo sulfonate substrates needed for the generation of the gem-di?uoro radical
, Angew. Chem., Int. Ed, p.14898, 2015.
, Acc. Chem. Res, vol.16, p.4570, 1461.
, Org. Biomol. Chem, issue.11, 2013.
, Org. Lett, 2013.
, Chem. Sci, vol.6, p.5426, 2015.