J. S. Cha, J. E. Kim, K. W. Lee, J. S. Cha, J. E. Kim et al., J. Org. Chem, vol.52, pp.5030-5032, 1987.

T. Soc-;-c)-yokoyama, N. Yamagata, A. O. Bedenbaugh, J. H. Bedenbaugh, W. A. Bergin et al., J. Am. Chem. Soc, vol.8, pp.5774-5775, 1970.

M. Muraki and T. Mukaiyama, Chem. Lett, vol.3, pp.1447-1450, 1974.

T. D. Hubert, D. P. Eyman, D. F. Wiemer, J. Org, J. S. Chem-;-cha et al., Bull. Korean Chem. Soc, vol.49, pp.3941-3944, 1981.

B. M. Trost, M. Zhang, N. Li, X. Tao, R. Ruzi et al., Comprehensive Organic Synthesis. Pergamon: Oxford, vol.8, issue.3, pp.259-305, 1991.

;. Commun, N. Sakai, K. Minato, Y. Ogiwara, T. Lett-;-c)-tokuyama et al., J. Braz. Chem. Soc, vol.53, pp.12-14, 1989.

T. Fukuyama, S. C. Lin, L. Li, P. Four, and F. Guibe, J. Am. Chem. Soc, vol.112, pp.4439-4445, 1981.

P. T. Ho and K. Y. Ngu, J. Org. Chem, vol.58, pp.2313-2316, 1993.

S. Chandrasekhar, M. S. Kumar, B. Muralidhar, T. Lett-;-i)-kangani, C. O. Kelley et al., Adv. Synth. Catal, vol.39, pp.1543-1546, 1983.

K. Nagayama, I. Shimizu, A. Yamamoto, L. J. Gooßen, K. Ghosh et al., Bull. Chem. Soc. Jap, vol.74, pp.3420-3424, 2001.

D. Addis, S. Das, K. Junge, and M. Beller, Angew. Chem. Int. Ed, vol.50, pp.6004-6011, 2011.

K. Miyamoto, Y. Motoyama, and H. Nagashima, Chem. Lett, vol.41, pp.229-231, 2012.

M. Castro, L. C. Li, H. Sortais, J. Darcel, C. Bézier et al., Catal. Sci. Technol, vol.48, issue.7, pp.2230-2234, 2012.

J. Zheng, S. Chevance, C. Darcel, J. Sortais, C. Wang et al., Chem. Commun, vol.49, pp.2307-2315, 2013.

R. J. Trovitch, R. J. Trovitch, and B. Royo, Recent advances in catalytic hydrosilylation of carbonyl groups mediated by well-defined first-row late transition metals, Advances in Organometallic Chemistry, vol.50, pp.1638-1642, 2014.

F. Kallmeier, R. Kempe, R. G. Harms, W. A. Herrmann, F. E. Kühn et al., Angew. Chem. Int. Ed, vol.57, 2018.

Y. Kuninobu, K. Takai, J. J. Kennedy-smith, K. A. Nolin, H. P. Gunterman et al., J. Mol. Catal. A: Chem, vol.296, pp.107-112, 1938.

C. K. Toh, Y. N. Sum, W. K. Fong, S. G. Ang, W. Y. Fan et al., Adv. Synth. Catal, vol.31, pp.4090-4098, 2012.

M. Tehfe, J. Lalevée, D. Gigmes, and J. P. Fouassier, In all cases, the selectivity 2:3 was above 94:6. 18. The reduction of crotonic (1y) and 3-methylcrotonic (1z) acids led after hydrolysis to butanal (5y) and 3-methylbutanal (5z) in 82% and 91% yield respectively, see S.I. 19, J. Polym. Sci., Part A: Polym. Chem, vol.48, pp.1830-1837, 2010.