, Chem. Eur. J, vol.61, pp.13064-13077, 2005.
, Acc. Chem. Res, vol.83, pp.2556-2568, 2017.
, Nat. Prod. Rep, vol.16, pp.597-606, 1999.
, J. Med. Chem, vol.53, pp.7902-7917, 2010.
, Angew. Chem., Int. Ed, vol.51, pp.720-723, 2012.
, Comprehensive Organic Synthesis, vol.1, pp.697-750, 2014.
, Org. Chem. Front, vol.3, pp.1535-1540, 2016.
, Org. Biomol. Chem, vol.16, pp.5767-5770, 2015.
,
, , vol.3, pp.1176-1179, 2018.
, Chem. Eur. J, vol.16, pp.4725-4728, 2010.
, Chem. Eur. J, vol.17, pp.313-315, 1999.
, Angew. Chem., Int. Ed, vol.26, pp.1798-1802, 2015.
, Org. Lett, vol.2, pp.795-797, 2000.
, J. Chem. Soc., Perkin Trans. 1, vol.13, pp.2479-2481, 1985.
, J. Fluorine Chem, vol.26, pp.271-276, 1965.
, , vol.3, pp.10731-10735, 2013.
, Tetrahedron Lett, vol.22, pp.5011-5014, 1981.
, Tetrahedron Lett, vol.34, pp.4623-4626, 1993.
, Tetrahedron Lett, vol.45, pp.967-970, 1970.
, Org. Lett, vol.19, pp.4672-4675, 2017.
, Tetrahedron Lett, pp.4169-4170, 1972.
, J. Am. Chem. Soc, vol.95, pp.4896-4904, 1973.
, J. Chem. Soc., Chem. Commun, pp.608-610, 1993.
, Beilstein J. Org. Chem, vol.13, pp.267-284, 2006.
, Angew. Chem., Int. Ed, vol.55, pp.3719-3723, 2016.
, Aust. J. Chem, vol.31, pp.2323-2326, 1978.
, J. Phys. Org. Chem, vol.13, pp.233-236, 2000.
, Org. Prep. Proced. Int, vol.24, pp.7-12, 1992.
, J. Am. Chem. Soc, vol.75, pp.5587-5590, 1953.
, J. Am. Chem. Soc, vol.76, pp.2203-2206, 1954.
,
, J. Chem. Soc., Perkin Trans. 1, vol.14, pp.5793-5794, 1952.
, Org. Lett, vol.18, pp.4300-4303, 2016.
,
, J. Am. Chem. Soc, vol.139, pp.16696-16707, 2017.
, J. Am. Chem. Soc, vol.140, pp.14421-14432, 2018.
,
308-311; d), Angew. Chem., Int. Ed, vol.477, pp.12274-12296, 2011. ,
, J. Am. Chem. Soc, vol.137, pp.9481-9488, 2015.
, J. Org. Chem, vol.82, pp.4993-4997, 2017.
, TURBOMOLE GmbH, since, 1989.
, This difference has to be attributed to three factors: i) the B3LYP formulation is not the same in TURBOMOLE and in Gaussioan09; ii) our basis set is somewhat larger; iii) we do not employ here an implicit solvent model
, J. Org. Chem, vol.52, pp.3901-3904, 1987.
, In studies on rhodium catalyzed transnitrilation of aryl boronic acids with DMMN the mechanism proposed involves the fragmentation of a ketenimine intermediate efficiently promoted by a strong base
, Under mild basic conditions (proton sponge) this intermediate is stable and can be hydrolyzed into a ketone, Angew. Chem., Int. Ed, vol.55, pp.326-330, 2016.
,
, Angew. Chem., Int, vol.56, pp.6999-7002, 2017.
, J. Chem. Phys, vol.38, pp.5648-5652, 1988.
, Phys. Rev. B, vol.123, pp.385-390, 1929.
, Can. J. Phys, vol.58, pp.1200-1211, 1980.
, Phys. Rev. Lett, vol.45, pp.3865-3868, 1992.
, J. Chem. Phys, vol.105, pp.9982-9985, 1996.
, J. Chem. Phys, p.154104, 2010.
, Theor. Chem. Acc, vol.120, pp.215-241, 2008.
, J. Chem. Phys, vol.118, pp.9095-9102, 2003.
, J. Chem. Phys, vol.132, p.231102, 2010.
, Phys. Chem. Chem. Phys, vol.9, 1921.
, Phys. Chem. Chem. Phys, vol.8, pp.1057-1065, 2006.
, Phys. Chem. Chem. Phys, vol.7, pp.3297-3305, 2005.
, Mol. Phys, vol.107, pp.963-975, 2009.
, Phys. Chem. Chem. Phys, vol.16, pp.16196-16203, 2014.
Fundamentals of Carbanion Chemistry, vol.1, 1965. ,
, Studies suggest that the phenyl group has a larger size than methyl, see: M. Charton, J. Am. Chem. Soc, vol.97, pp.1552-1556, 1975.
,
, J. Am. Chem. Soc, vol.122, pp.1567-1572, 2000.
, Acta Chem. Scand., Ser. B, vol.28, pp.705-710, 1974.
, For an estimation of electronegativity of the MgBr group, Chem. Lett, pp.1003-1006, 1982.
, J. Phys. Chem, vol.69, pp.3284-3289, 1965.
, Chem. Ber, vol.129, pp.1335-1344, 1996.
, J. Am. Chem. Soc, vol.115, pp.11353-11357, 1993.
, Organometallics, vol.17, pp.3512-3515, 1998.
, J. Chem. Sci, vol.128, pp.1597-1606, 2016.
, Lithium Compounds in Organic Synthesis, pp.3-31, 2014.
, Chem. Eur. J, vol.15, pp.7130-7178, 2009.
, Chem. Rev, vol.116, pp.5642-5687, 2016.
, Indian J. Chem, vol.40, pp.939-945, 1980.
, J. Org. Chem, vol.55, pp.1479-1483, 1990.
, Div. Chem. Sci, vol.17, pp.2518-2520, 1991.
, , vol.58, 1957.
, , vol.16, pp.7815-7819, 2018.