, Heterocyclic Chemistry, 1996.
, Nat. Prod. Rep, vol.14, pp.435-446, 1997.
, Chem. Rev, vol.104, pp.2127-2198, 2004.
For representative examples, see: a) ,
, Angew. Chem. Int. Ed, vol.50, pp.8876-8880, 1985.
, For representative review, vol.124, pp.1410-1459, 2007.
, For a representative review, see: F.-X. Felpin, Eur. J. Org. Chem, pp.3693-3712, 2003.
, Angew. Chem. Int. Ed, vol.55, pp.1864-1867, 2016.
, Adv. Synth. Catal, vol.128, pp.3525-3529, 2016.
, Chem. Rev, vol.98, pp.1158-1167, 1901.
, International Review of Cytology, vol.213, pp.1-47, 2002.
, Arch. Oral. Biol, vol.32, pp.607-610, 1987.
, J. Biol. Chem, p.832, 1959.
, Int. J. Clin. Exp. Pathol, vol.8, pp.7978-7987, 2015.
6217-6254; b) B. Plietker, Iron catalysis in organic chemistry: reactions and applications, Chem. Soc. Rev, vol.104, pp.2282-2291, 2004. ,
, Iron Catalysis II, vol.111, pp.3170-3387, 2010.
, J. Org. Chem, vol.35, pp.1383-1398, 2015.
, Isr. J. Chem, vol.57, pp.1151-1159, 2017.
753-819; for selected exemples of recent catalyzed reductive amination, see: b), Adv. Synth. Catal, vol.352, pp.326-332, 2010. ,
, Nature Commun, vol.9, pp.1235-1240, 2018.
, Angew. Chem. Int. Ed, vol.49, pp.1687-1693, 2008.
, , vol.6, pp.381-388, 2016.
, J. Org. Chem, vol.22, pp.5985-5990, 2015.
, , vol.8, pp.6440-6445, 2018.
, Org. Lett, vol.19, pp.6-9, 2016.
, Eur. J. Inorg. Chem, vol.9, pp.3546-3550, 2010.
The handbook of homogeneous hydrogenation, 2007. ,
, Acc. Chem. Res, vol.74, pp.97-102, 1974.
, Chem. Soc. Rev, vol.27, pp.395-404, 1998.
, Appl. Organomet. Chem, vol.24, pp.751-757, 2010.
, Angew. Chem. Int. Ed, vol.52, pp.8045-8049, 2013.
, Isr. J. Chem, vol.125, pp.1216-1221, 2013.
, ChemCatChem, vol.6, pp.763-766, 2014.
, Chem. Commun, vol.50, pp.14229-14232, 2014.
, Organometallics, vol.32, pp.893-897, 2013.
, Organometallics, vol.35, pp.2930-2937, 2016.
, Noticeably, the reaction of p-methoxybenzylidenebenzimide with 2 equiv. of phenylsilane in toluene at 100 °C for 4 h led to only 14% of (pmethoxybenzylphenylamine. The same reaction in the presence of 1 equiv
, The reductive amination reaction of benzaldehyde with butylamine in the presence of 2 equiv. of phenylsilane and 1 equiv. of carboxylic acid (acetic or valeric) led to the imine as the major product (70-75% yields) with dibenzylbutylamine and N-benzyl-N-butylcarbamides as the byproducts whereas without carboxylic acid
, Angew. Chem. Int. Ed, vol.52, pp.11577-11580, 2013.
, J. Am. Chem. Soc, vol.125, pp.3659-3661, 1972.
, Eur. J. Org. Chem, vol.134, p.18325, 2011.
, Angew. Chem, vol.121, pp.9671-9674, 2009.
, Angew. Chem. Int. Ed, vol.48, pp.9675-9678, 2009.
, Angew. Chem. Int
, Angew. Chem, vol.48, pp.1694-1698, 2009.
, Angew. Chem. Int. Ed, vol.51, pp.1662-1666, 2012.