It’s not a mystery! Apart the steric factors, thermodynamic factors (like in this case) may also influence the stereoselectivity of a reaction, by favoring the stereospecific transition state that is more thermodynamically stable. Furthermore, stereoselective organometallic catalysts may interfere to both steric and thermodynamic factors and lead to the desired steroselectivity. Indicatively, see:
1). The Henry reaction: recent examples, Tetrahedron, (2001), 57, 915-945, (2001)
http://chemistry.mdma.ch/hiveboard/picproxie_docs/000448477-04082418194214626.pdf2). Unveiling Reliable Catalysts for the Asymmetric Nitroaldol (Henry) Reaction, Angew.Chem., Int.Ed., 43, 5442-5444, (2004)
http://www.uwindsor.ca/people/jgreen/sites/uwindsor.ca.people.jgreen/files/acie-2005-43-5442-palomo.pdf3). Salicylaldimine based copper (II) complex-potential catalyst for asymmetric Henry reaction, ARKIVOC, 2010(11), 370-379, (2010)
https://quod.lib.umich.edu/cgi/p/pod/dod-idx/salicylaldimine-based-copper-ii-complex-potential-catalyst.pdf?c=ark;idno=5550190.0011.b30;format=pdf4). Organocatalytic Enantioselective Henry Reactions, Symmetry, 3, 220-245, (2011)
http://citeseerx.ist.psu.edu/viewdoc/download?doi=10.1.1.698.1496&rep=rep1&type=pdf5). Advances in Contemporary Research, Asymmetric Henry reaction catalysed by transition metal complexes: A short review, Indian Journal of Chemistry-Advances in Contemporary Research, 52B, 87-108, (2013)
http://nopr.niscair.res.in/bitstream/123456789/15621/1/IJCB%2052B%281%29%2087-108.pdf