Arlette Solladié-Cavallo, Ph.D. - Publications

Affiliations: 
École européenne de chimie, polymères et matériaux, University of Strasbourg 
Area:
organic chemistry, stereoselective synthesis, NMR

45 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2010 SOLLADIE-CAVALLO A, BONNE F. ChemInform Abstract: Synthesis of Enantiomerically Pure threo-1-Alkyl-2- benzyloxypropylamines. Cheminform. 27: no-no. DOI: 10.1002/chin.199621078  0.437
2010 SOLLADIE-CAVALLO A, QUAZZOTTI S. ChemInform Abstract: An Efficient Synthesis of (+)-8-Phenylmenthyl Isocyanoacetate. Cheminform. 23: no-no. DOI: 10.1002/chin.199217243  0.301
2006 Pažický M, Gášpár B, Solladié-Cavallo A, Sališová M, Bohá? A, Hutta M, Addová G. The epimerization of chiral α-amino acids by 2-hydroxy-2-methyl-1- tetralone template - The synthesis, conditions and mechanism of isomerization Synthesis. 2013-2018. DOI: 10.1055/s-2006-942401  0.352
2006 Solladié-Cavallo A, Choucair E, Balaz M, Lupattelli P, Bonini C, Di Blasio N. A mild stereo- and enantiospecific conversion of 2,3-diaryl-substituted oxiranes into 2,2-dimethyl-1,3-dioxolanes by an acetone/amberlyst 15 system European Journal of Organic Chemistry. 3007-3011. DOI: 10.1002/Ejoc.200600034  0.603
2005 Solladié-Cavallo A, Lupattelli P, Bonini C. Regio- and stereoselective ring opening of 2,3-diaryl oxiranes by LiBr/Amberlyst 15: a new stereocontrolled access to 1,2-diaryl-2-bromo alcohols. The Journal of Organic Chemistry. 70: 1605-11. PMID 15730278 DOI: 10.1021/jo048045w  0.366
2004 Solladié-Cavallo A, Roje M, Giraud-Roux M, Chen Y, Berova N, Sunjic V. Trans-diaryl epoxides: asymmetric synthesis, ring-opening, and absolute configuration. Chirality. 16: 196-203. PMID 14770417 DOI: 10.1002/Chir.20005  0.33
2004 Solladié-Cavallo A, Jierry L, Lupattelli P, Bovicelli P, Antonioletti R. Cyclohexanones derived from dihydrocarvone as precursor of chiral dioxiranes for epoxidation of olefins Tetrahedron. 60: 11375-11381. DOI: 10.1016/j.tet.2004.09.089  0.392
2003 Solladié-Cavallo A, Balaz M, Salisova M, Welter R. New 1,3-oxathianes derived from myrtenal: synthesis and reactivity. The Journal of Organic Chemistry. 68: 6619-26. PMID 12919025 DOI: 10.1021/Jo034404W  0.621
2003 Solladié-Cavallo A, Balaz M, Salisova M. Diastereoreactivity of a chiral oxathiane derived from 5-hydroxy-1-tetralone European Journal of Organic Chemistry. 337-345. DOI: 10.1002/Ejoc.200390039  0.567
2002 Solladié-Cavallo A, Lupattelli P, Marsol C, Isarno T, Bonini C, Caruso L, Maiorella A. Opening of diaryl epoxides: Ortho-fluorophenyl and 2-pyridyl epoxides European Journal of Organic Chemistry. 1439-1444.  0.325
2002 Solladié-Cavallo A, Sedy O, Salisova M, Schmitt M. Stereodifferentiation in a chiral 1,4-oxazin-2-one derived from 2-hydroxy-2-methyl-1-tetralone - A reagent for deracemization of amino acids European Journal of Organic Chemistry. 3042-3049.  0.32
2001 Solladié-Cavallo A, Sedy O, Salisova M, Biba M, Welch CJ, Nafié L, Freedman T. A chiral 1,4-oxazin-2-one: Asymmetric synthesis versus resolution, structure, conformation and VCD absolute configuration Tetrahedron Asymmetry. 12: 2703-2707. DOI: 10.1016/S0957-4166(01)00478-5  0.34
2001 Solladié-Cavallo A, Balaz M, Salisova M, Suteu C, Nafie LA, Cao X, Freedman TB. A new chiral oxathiane: Synthesis, resolution and absolute configuration determination by vibrational circular dichroism Tetrahedron Asymmetry. 12: 2605-2611. DOI: 10.1016/S0957-4166(01)00441-4  0.569
2000 Solladie-Cavallo A, Bouerat L. Epoxidation of p-methoxycinnamates using chiral dioxiranes derived from new trisubstituted halogenated cyclohexanones: enhanced efficiency of ketones having an axial halogen Organic Letters. 2: 3531-4. PMID 11073637  0.304
2000 Solladié-Cavallo A, Bouérat L. 2-Chloro and 2-fluoro ketones derived from the chiral-pool Tetrahedron Asymmetry. 11: 935-941. DOI: 10.1016/S0957-4166(00)00013-6  0.395
2000 Solladié-Cavallo A, Bouérat L, Roje M. Asymmetric synthesis of trans-disubstituted aryl-vinyl epoxides: a p-methoxy effect Tetrahedron Letters. 41: 7309-7312. DOI: 10.1016/S0040-4039(00)01222-3  0.376
2000 Solladie-Cavallo A, Bouerat L, Roje M. ChemInform Abstract: Asymmetric Synthesis of trans-Disubstituted Aryl-Vinyl Epoxides: A p-Methoxy Effect. Cheminform. 31: no-no. DOI: 10.1002/chin.200050110  0.396
2000 Solladié-Cavallo A, Crescenzi B. Full conversion in diastereoselective aldol additions using 'naked' enolates under catalytic amount of phosphazene base: The hydroxypinanone as chiral auxiliary Synlett. 327-330.  0.331
1998 Solladié-Cavallo A, Diep-Vohuule A, Isarno T. Two-Step Synthesis of trans-2-Arylcyclopropane Carboxylates with 98-100 % ee by the Use of a Phosphazene Base. Angewandte Chemie (International Ed. in English). 37: 1689-1691. PMID 29711518 DOI: 10.1002/(SICI)1521-3773(19980703)37:12<1689::AID-ANIE1689>3.0.CO;2-9  0.427
1998 Solladié-Cavallo A, Schwarz J, Mouza C. A three-step, highly enantioselective synthesis of (R)-2-methyl tryptophane ethyl ester: Comparison with chemical resolution Tetrahedron Letters. 39: 3861-3864. DOI: 10.1016/S0040-4039(98)00633-9  0.34
1998 Roje M, Vinkovi? V, Šunji?? V, Solladié-Cavallo A, Diep-Vohuule A, Isarno T. Stereoselective cyclopropanation and ring-opening: Application to the synthesis of pure (S)-2-methyl-3-arylpropylamines Tetrahedron. 54: 9123-9128. DOI: 10.1016/S0040-4020(98)00549-3  0.345
1998 Solladié-Cavallo A, Diep-Vohuule A, Isarno T. Two-step synthesis of trans-2-arylcyclopropane carboxylates with 98-100% ee by the use of a phosphazene base Angewandte Chemie - International Edition. 37: 1689-1691. DOI: 10.1002/(SICI)1521-3773(19980703)37:12<1689::AID-ANIE1689>3.0.CO;2-9  0.358
1996 Solladié-Cavallo A, Bonne F. Synthesis of Enantiomerically Pure Threo 1-Alkyl-2-benzyloxy-propylamines Tetrahedron Asymmetry. 7: 171-180. DOI: 10.1016/0957-4166(95)00433-5  0.432
1994 Solladié-Cavallo A, Csaky AG, Gantz I, Suffert J. Diastereoselective alkylation of 8-phenylmenthyl phenylacetate: Aggregated lithium enolate versus "naked" enolate Journal of Organic Chemistry. 59: 5343-5346. DOI: 10.1021/Jo00097A041  0.596
1994 Solladié-Cavallo A, Schwarz J, Burger V. A four-step, highly enantioselective synthesis and enzymatic resolution of 3,4-dichloro-phenylalanine. Tetrahedron: Asymmetry. 5: 1621-1626. DOI: 10.1016/0957-4166(94)80133-9  0.351
1994 Solladié-Cavallo A, Csaky AG. Stereochemistry of silyl ketene acetals of some 8-phenylmenthyl arylacetates Journal of Organic Chemistry. 59: 2585-2589.  0.616
1994 Solladié-Cavallo A, Koessler JL. A four-step diastereoselective synthesis of D-erythro-sphingosine by an enantioselective aldol reaction using a titanium enolate derived from a chiral iminoglycinate Journal of Organic Chemistry. 59: 3240-3242.  0.413
1993 Solladié-Cavallo A, Bencheqroun M, Bonne F. Lithium aluminum amides : New reagents for the synthesis of imines Synthetic Communications. 23: 1683-1687. DOI: 10.1080/00397919308011266  0.351
1992 Solladié-Cavallo A, Quazzotti S, Fischer J, DeCian A. Threo aryl trifluoromethyl chlorohydrins: Synthesis, reactivity, and structure Journal of Organic Chemistry. 57: 174-178.  0.304
1992 Solladié-Cavallo A, Bencheqroun M. Inexpensive reagents for the synthesis of amides from esters and for regioselective opening of epoxides Journal of Organic Chemistry. 57: 5831-5834.  0.447
1991 Solladié-Cavallo A, Bencheqroun M. Diastereoselective reduction of an α-keto-ester derived from (-)-8-phenylmenthol: A 4-step synthesis of R-Halostachine analogue. Tetrahedron: Asymmetry. 2: 1165-1171. DOI: 10.1016/S0957-4166(00)82014-5  0.352
1991 Solladié-Cavallo A, Bencheqroun M. Chiral arene-chromium-tricarbonyl complexes: a 2-step synthesis of halostachin analogues Journal of Organometallic Chemistry. 406: C15-C19. DOI: 10.1016/0022-328X(91)83129-R  0.333
1990 SOLLADIE-CAVALLO A, QUAZZOTTI S. ChemInform Abstract: 1,1-Dichloro-2,2,2-trifluoroethylzinc and Lithium Compounds in Asymmetric Synthesis. Cheminform. 21. DOI: 10.1002/chin.199027277  0.317
1990 SOLLADIE-CAVALLO A. ChemInform Abstract: Chiral Arene-Chromium Carbonyl Complexes in Asymmetric Synthesis Cheminform. 21. DOI: 10.1002/chin.199012366  0.359
1987 Solladié-Cavallo A, Lapitajs G, Buchert P, Klein A, Colonna S, Manfredi A. Asymmetric synthesis of ephedrine analogs Journal of Organometallic Chemistry. 330: 357-363. DOI: 10.1016/S0022-328X(00)99049-1  0.345
1986 Solladie-Cavallo A, Farchani D. Enantioselective synthesis of chiral benzylic amines. (A stereospecific transamination-alkylation reaction) Tetrahedron Letters. 27: 1331-1334. DOI: 10.1016/S0040-4039(00)84251-3  0.443
1983 Solladié-Cavallo A, Haesslein JL. Asymmetric palladium-assisted alkylation of alkenes Helvetica Chimica Acta. 66: 1760-1773. DOI: 10.1002/hlca.19830660615  0.406
1982 Solladié-Cavallo A, Haesslein JL, Bäckvall JE. Asymmetric palladium-assisted alkylation of olefins Tetrahedron Letters. 23: 939-942. DOI: 10.1016/S0040-4039(00)86988-9  0.409
1982 Solladié G, Greck C, Demailly G, Solladié-Cavallo A. Reduction of β-ketosulfoxides : a highly efficient asymmetric synthesis of both enantiomers of methyl carbinols from the corresponding esters Tetrahedron Letters. 23: 5047-5050. DOI: 10.1016/S0040-4039(00)85569-0  0.354
1981 SOLLADIE-CAVALLO A, SUFFERT J, HAESSLEIN J. ChemInform Abstract: NEW ARENE(DICARBONYL)CHROMIUM CHELATES: APPLICATION TO THE ASYMMETRICAL SYNTHESES OF AMINES Chemischer Informationsdienst. 12. DOI: 10.1002/chin.198111291  0.305
1980 Solladié-Cavallo A, Suffert J, Haesslein J. New Arene(dicarbonyl)chromium Chelates: Application to Asymmetric Synthesis of Amines Angewandte Chemie International Edition in English. 19: 1005-1006. DOI: 10.1002/anie.198010051  0.308
1980 Solladié-Cavallo A, Suffert J, Haesslein J. Neue Aren(dicarbonyl)chrom-Chelate: Verwendung zur asymmetrischen Synthese von Aminen Angewandte Chemie. 92: 1038-1039. DOI: 10.1002/ange.19800921209  0.347
1978 Mioskowski C, Solladie-Cavallo A, Solladie G. Double asymmetric induction in benchrotrene derivatives Journal of Organometallic Chemistry. 149: C63-C65. DOI: 10.1016/S0022-328X(00)90410-8  0.35
1978 MIOSKOWSKI C, SOLLADIE-CAVALLO A, SOLLADIE G. ChemInform Abstract: DOUBLE ASYMMETRIC INDUCTION IN BENCHROTRENE DERIVATIVES Chemischer Informationsdienst. 9. DOI: 10.1002/chin.197832103  0.323
1968 Brauman JI, Solladié-Cavallo A. Stereospecific Friedel-Crafts reactions: Alkylation with a cyclic ether Chemical Communications (London). 1124-1125. DOI: 10.1039/C19680001124  0.497
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