R. C. Fuson and B. A. Bull, The Haloform Reaction., Chemical Reviews, vol.15, issue.3, pp.275-309, 1934.
DOI : 10.1021/cr60052a001

A. Kong, R. Engel, and . Bull, A Mechanistic Investigation of the Todd Reaction, Bulletin of the Chemical Society of Japan, vol.58, issue.12, pp.3671-3672, 1985.
DOI : 10.1246/bcsj.58.3671

K. Troev, E. M. Kirilov, and D. M. Roundhill, A Study of the Atherton???Todd Reaction Mechanism, Bulletin of the Chemical Society of Japan, vol.63, issue.4, pp.1284-1285, 1990.
DOI : 10.1246/bcsj.63.1284

M. I. Antczak and J. Montchamp, Mild Synthesis of Organophosphorus Compounds:?? Reaction of Phosphorus-Containing Carbenoids with Organoboranes, Organic Letters, vol.10, issue.5, pp.977-980, 2008.
DOI : 10.1021/ol800085u

R. Hulst, B. L. Feringa, and N. K. De-vries, The31P-NMR Spectroscopic Determination of the Enantiomeric Excess of Unprotected Amino Acids, Angewandte Chemie International Edition in English, vol.17, issue.8, pp.1092-1093, 1992.
DOI : 10.1002/anie.199210921

R. Hulst, R. M. Kellogg, and B. L. Feringa, New methodologies for enantiomeric excess (ee) determination based on phosphorus NMR, Recueil des Travaux Chimiques des Pays-Bas, vol.28, issue.4-5, pp.115-138, 1995.
DOI : 10.1002/recl.19951140402
URL : https://www.rug.nl/research/portal/files/3621698/1995ReclTravChimPaysBasHulst1.pdf

R. Hulst, R. W. Zijlstra, B. L. Feringa, N. K. De-vries, W. Ten-hoeve et al., A new 31P NMR method for the enantiomeric excess determination of alcohols, amines and amino acid esters, Tetrahedron Letters, vol.34, issue.8, pp.1339-1342, 1993.
DOI : 10.1016/S0040-4039(00)91790-8

R. Hulst, R. W. Zijlstra, N. K. De-vries, and B. L. Feringa, (S)-2H-2-oxo-5,5-dimethyl-4(R)-phenyl-1,3,2-dioxaphosphorinane, a new reagent for the enantiomeric excess determination of unprotected amino acids using 31P NMR, Tetrahedron: Asymmetry, vol.5, issue.9, pp.1701-1710, 1994.
DOI : 10.1016/0957-4166(94)80081-2

R. J. Corriu, G. F. Lanneau, and D. Leclercq, Investigations of the nucleophilic displacement at the tetrahedral phosphorus - kinetic effects of the nucleophile for a given stereochemistry, Tetrahedron, vol.42, issue.20, pp.5591-5600, 1986.
DOI : 10.1016/S0040-4020(01)88163-1

L. P. Reiff and H. S. Aaron, Stereospecific synthesis and reactions of optically active isopropyl methylphosphinate, Journal of the American Chemical Society, vol.92, issue.17, pp.5275-5276, 1970.
DOI : 10.1021/ja00720a077

W. Stec and M. Mikolajczyk, Stereochemistry of organophosphorus cyclic compounds???II, Tetrahedron, vol.29, issue.3, pp.539-54680006, 1973.
DOI : 10.1016/0040-4020(73)80006-7

G. Mielniczak and A. Bopusi?ski, Iodoform, a New Reagent in the Todd-Atherton Reaction, Synthetic Communications, vol.45, issue.22, pp.3851-3859, 2003.
DOI : 10.1016/0040-4020(73)80212-1

A. K. Szardenings, M. F. Gordeev, and D. V. Patel, A general and convenient synthesis of novel phosphotyrosine mimetics, Tetrahedron Letters, vol.37, issue.21, pp.3635-363810, 1996.
DOI : 10.1016/0040-4039(96)00666-1

L. J. Silverberg, J. L. Dillon, and P. Vemishetti, A simple, rapid and efficient protocol for the selective phosphorylation of phenols with dibenzyl phosphite, Tetrahedron Letters, vol.37, issue.6, pp.771-774, 1996.
DOI : 10.1016/0040-4039(95)02294-5

L. K. Lukanov, A. P. Venkov, and N. M. Mollov, The Application of Phase-Transfer Catalyzed Version of Atherton-Todd Reaction to Sulfonamides, Synthetic Communications, vol.28, issue.7, pp.767-773, 1986.
DOI : 10.1080/00397918608059656

I. Bonnaventure and A. B. Charrette, -Phosphinoylimines: Discovery of New Effective Chiral Ligands, The Journal of Organic Chemistry, vol.73, issue.16, pp.6330-6340, 2008.
DOI : 10.1021/jo800969x
URL : https://hal.archives-ouvertes.fr/halshs-00308613

K. P. Jayasundera, A. J. Watson, and C. M. Taylor, Synthesis of a tetrasubstituted arylphosphonate via the anionic phospho-Fries rearrangement, Tetrahedron Letters, vol.46, issue.25, pp.4311-4313, 2005.
DOI : 10.1016/j.tetlet.2005.04.104

Y. Ding and X. Huang, THE HIGH STEREOSELECTIVE SYNTHESIS OF ??-ALKYNYL-ENOL PHOSPHATES, Synthetic Communications, vol.34, issue.3, pp.449-454, 2001.
DOI : 10.1081/SCC-100000538

T. Shioiri, S. Ninomiya, and S. Yamada, Diphenylphosphoryl azide. New convenient reagent for a modified Curtius reaction and for peptide synthesis, Journal of the American Chemical Society, vol.94, issue.17, pp.6203-6205, 1972.
DOI : 10.1021/ja00772a052

Q. Cai, G. He, and D. Ma, Mild and Nonracemizing Conditions for Ullmann-type Diaryl Ether Formation between Aryl Iodides and Tyrosine Derivatives, The Journal of Organic Chemistry, vol.71, issue.14, pp.5268-5273, 2006.
DOI : 10.1021/jo0606960

Y. Hamada and T. Shioiri, Recent Progress of the Synthetic Studies of Biologically Active Marine Cyclic Peptides and Depsipeptides, Chemical Reviews, vol.105, issue.12, pp.4441-4482, 2005.
DOI : 10.1021/cr0406312

S. Yamada, Y. Kasai, and T. Shioiri, Diethylphosphoryl cyanide. A new reagent for the synthesis of amides., Tetrahedron Letters, vol.14, issue.18, pp.1595-1598, 1973.
DOI : 10.1016/S0040-4039(01)96005-8

R. J. Cremlyn, Some reactions of O,O-diphenylphosphoryl azide, Australian Journal of Chemistry, vol.26, issue.7, pp.1591-1593, 1973.
DOI : 10.1071/CH9731591

E. Shi, C. Pei, and . Phosphorus, Synthesis of Phosphorocyanidates via Phosphorochloridates, Phosphorus, Sulfur, and Silicon and the Related Elements, vol.50, issue.5, pp.1093-1099, 2003.
DOI : 10.1021/jo01149a031

E. Shi and C. Pei, Phase???Transfer Catalyzed Pseudohalogenation of Phosphorochloridates, Synthetic Communications, vol.72, issue.5, pp.669-673, 2005.
DOI : 10.1021/jo01149a031

A. Bartoszewicz, M. Kalek, and J. Stawinski, -Phosphonoselenoate Monoesters: Mechanistic and Synthetic Studies, The Journal of Organic Chemistry, vol.73, issue.13, pp.5029-5038, 2008.
DOI : 10.1021/jo8006072
URL : https://hal.archives-ouvertes.fr/hal-00550288

L. I. Minaeva, L. S. Patrikeeva, M. M. Kabachnik, and I. P. Beletskaya, Phosphorylation of Amino(aryl)methylphosphonates by the Atherton???Todd Reaction, Russian Journal of Organic Chemistry, vol.46, issue.10, pp.1579-1580, 2010.
DOI : 10.1134/S1070428010100246

R. I. Duclos, . Jr, D. Lu, J. Guo, and A. Makriyannis, Synthesis and characterization of 2-substituted bornane pharmacophores for novel cannabinergic ligands, Tetrahedron Letters, vol.49, issue.39, pp.5587-5589, 2008.
DOI : 10.1016/j.tetlet.2008.07.029

T. Yang, C. Lin, H. Fu, Y. Jiang, and Y. Zhao, Copper-Catalyzed Synthesis of Medium- and Large-Sized Nitrogen Heterocycles via N-Arylation of Phosphoramidates and Carbamates, Organic Letters, vol.7, issue.21, pp.4781-4784, 2005.
DOI : 10.1021/ol052126c

A. B. Chopa, M. T. Lockhart, and G. Silbestri, Two-Step Synthesis of Arylstannanes from Phenols, Organometallics, vol.19, issue.12, pp.2249-2250, 2000.
DOI : 10.1021/om000013l

N. Yoshikai, H. Matsuda, and E. Nakamura, Hydroxyphosphine Ligand for Nickel-Catalyzed Cross-Coupling through Nickel/Magnesium Bimetallic Cooperation, Journal of the American Chemical Society, vol.131, issue.27, pp.9590-9599, 2009.
DOI : 10.1021/ja903091g

B. Dhawan and D. Redmore, o-Hydroxyaryl diphosphonic acids, The Journal of Organic Chemistry, vol.49, issue.21, pp.4018-4021, 1984.
DOI : 10.1021/jo00195a029

L. S. Melvin, An efficient synthesis of 2-hydroxyphenylphosphonates, Tetrahedron Letters, vol.22, issue.35, pp.3375-3376, 1981.
DOI : 10.1016/S0040-4039(01)81909-2

C. M. Taylor and A. J. Watson, The Anionic Phospho-Fries Rearrangement, Current Organic Chemistry, vol.8, issue.7, pp.623-636, 2004.
DOI : 10.2174/1385272043370717

S. E. Denmark and T. Bui, Asymmetric Catalysis Special Feature Part I: Chiral phosphoramide-catalyzed, enantioselective, directed cross-aldol reactions of aldehydes, Proceedings of the National Academy of Sciences, vol.54, issue.8, pp.5439-5444, 2004.
DOI : 10.1021/ja025670e
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC397401

R. Hulst, H. Heres, N. C. Peper, and R. M. Kellogg, Synthesis and application of new chiral ligands for the asymmetric borane reduction of prochiral ketones, Tetrahedron: Asymmetry, vol.7, issue.5, pp.1373-1384, 1996.
DOI : 10.1016/0957-4166(96)00154-1

R. Hulst, H. Heres, K. Fitzpatrick, N. C. Peper, and R. M. Kellogg, Catalytic enantioselective alkylation of benzaldehyde with diethylzinc using chiral nonracemic (thio)-phosphoramidates, Tetrahedron: Asymmetry, vol.7, issue.9, pp.2755-2760, 1996.
DOI : 10.1016/0957-4166(96)00355-2

A. Granzow, Flame retardation by phosphorus compounds, Accounts of Chemical Research, vol.11, issue.5, pp.177-183, 1978.
DOI : 10.1021/ar50125a001

D. M. Jones and T. M. Noone, Some approaches to the permanent flameproofing of cotton: Systems containing phosphorus, Journal of Applied Chemistry, vol.83, issue.9, pp.397-405, 1962.
DOI : 10.1002/jctb.5010120904

P. Midoux, C. Pichon, J. Yaouanc, and P. Jaffrès, Chemical vectors for gene delivery: a current review on polymers, peptides and lipids containing histidine or imidazole as nucleic acids carriers, British Journal of Pharmacology, vol.3, issue.2, pp.166-178, 2009.
DOI : 10.1111/j.1476-5381.2009.00288.x
URL : https://hal.archives-ouvertes.fr/hal-00525108

C. R. Safinya, Structures of lipid???DNA complexes: supramolecular assembly and gene delivery, Current Opinion in Structural Biology, vol.11, issue.4, pp.440-448, 2001.
DOI : 10.1016/S0959-440X(00)00230-X

R. Zeng, H. Fu, and Y. Zhao, Synthesis of Novel Biomimetic Zwitterionic Phosphorylcholine-Bound Chitosan Derivative, Macromolecular Rapid Communications, vol.124, issue.7, pp.548-552, 2006.
DOI : 10.1002/marc.200500876

L. Yang, R. Zeng, C. Li, G. Li, R. Qiao et al., Novel synthesis and in vitro drug release of polymeric prodrug: Chitosan???O-isopropyl-5???-O-d4T monophosphate conjugate, Bioorganic & Medicinal Chemistry Letters, vol.19, issue.9, pp.2566-2569, 2009.
DOI : 10.1016/j.bmcl.2009.03.044

L. Yang, L. Chen, R. Zeng, C. Li, R. Qiao et al., Synthesis, nanosizing and in vitro drug release of a novel anti-HIV polymeric prodrug: Chitosan-O-isopropyl-5???-O-d4T monophosphate conjugate, Bioorganic & Medicinal Chemistry, vol.18, issue.1, pp.117-123, 2010.
DOI : 10.1016/j.bmc.2009.11.013