B. S. Lucas, S. D. Burke, O. Lett, V. B. Birman, H. Jiang et al., Palladium(0)-Mediated Desymmetrization of Meso Tetraols:??? An Approach to the C3???C17 Bis-oxane Segment of Phorboxazoles A and B, Organic Letters, vol.5, issue.21, p.3915, 2003.
DOI : 10.1021/ol0354775

O. Parrain, C. Chuzel, . Bressy, . Org, and . Lett, 17, 2118; for a review in the context of total synthesis: e), 1938.

T. =. Pyridine and . Tetrahydrofuran, Scheme 5 Total synthesis of (+ +)-cryptocaryalactone. DBU = 1,8- diazabicyclo[5-4-0]undec-7-ene

. Angew, J. A. Chem, J. Enquist, and B. M. Stoltz, Enolates: i), Nature, vol.121, issue.453, p.1228, 2008.

R. Gurubrahamam, Y. Cheng, W. Huang, K. Chen, H. Pellissier et al., Catalytic Kinetic Resolution, in Separation of Enantiomers: New Methods and Applications Regio-and Position Selective Reactions and Desymmetrizations in Comprehensive Enantioselective Organocatalysis 121, 9076; for reviews on chiral isothioureas as organocatalysts, see: b), Ed.: P. I. Dalko), Wiley-VCH, pp.86-96, 1613.

H. Clavier, F. Caijo, E. Borrÿ, D. Rix, F. Boeda et al., Unlike catalyst 5, classical metathesis catalysts lead to a mixture of products for this transformation, Eur. J. Org. Chem, pp.4254-4265, 2009.

H. H. Meyer, L. A. Mori, H. Furukawa, G. Sabitha, V. Bhaskar et al., 13 steps); d) steps); f) P steps); g), Chem. Pharm. Bull. Tetrahedron Beilstein J. Org. Chem. Helv. Chim. Acta Tetrahedron Lett, vol.42, issue.53, pp.977-981, 1984.

R. N. Saicic, For reviews, Tetrahedron Nat. Chem, vol.2014, issue.1, pp.8183-8218, 2006.

M. E. Abbasov, D. Romo-b-)-e, R. P. Marquÿs-lûpez, M. Herrera, and . Christmann, The ever-expanding role of asymmetric covalent organocatalysis in scalable, natural product synthesis, For reviews about total syntheses involving an enantioselective organocatalysis, pp.1318-1327, 2007.
DOI : 10.1002/anie.201207949