Arlette Solladié-Cavallo, Ph.D. - Publications

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

92 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
2007 Solladié-Cavallo A, Marsol C, Azyat K, Roje M, Welch C, Chilenski J, Taillasson P, D'Orchymont H. Enantiopure (9-anthryl)(2-piperidyl)- and (9-anthryl)(2-pyridyl)methanols - Their use as chiral modifiers for heterogeneous hydrogenation of keto esters over Pt/Al2O3 European Journal of Organic Chemistry. 826-830. DOI: 10.1002/ejoc.200600734  1
2006 Solladié-Cavallo A, Lupattelli P, Bonini C, Ostuni V, Blasio ND. New aniline-containing amino alcohols from trans-(R,R)-2-(2-nitrophenyl)-3-phenyloxirane as useful intermediates for the synthesis of chiral ligands, bases, and benzoxazine nucleus. The Journal of Organic Chemistry. 71: 9891-4. PMID 17168617 DOI: 10.1021/jo0617969  1
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  1
2006 Solladié-Cavallo A, Azyat K, Jierry L, Cahard D. A new tetrasubstituted α-fluoro cyclohexanone bearing a fluoroisopropyl group at C5 Journal of Fluorine Chemistry. 127: 1510-1514. DOI: 10.1016/j.jfluchem.2006.06.021  1
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  0.84
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  1
2005 Solladié-Cavallo A, Azyat K, Schmitt M, Welter R. Enantiopure erythro- and threo-1-aryl-1-[2-pyrrolidyl]-methanols: Synthesis from L-proline Tetrahedron Asymmetry. 16: 1055-1060. DOI: 10.1016/j.tetasy.2005.01.010  1
2005 Solladié-Cavallo A, Ahmed B, Schmitt M, Garin F. Heterogeneous hydrogenation of 1-naphtol and 2-naphtol over Ru/Al2O3: A simple 1H NMR method for determination of the diastereoselectivity Comptes Rendus Chimie. 8: 1975-1980. DOI: 10.1016/j.crci.2005.06.005  1
2004 Freedman TB, Cao X, Nafie LA, Solladié-Cavallo A, Jierry L, Bouerat L. VCD configuration of enantiopure/-enriched tetrasubstituted alpha-fluoro cyclohexanones and their use for epoxidation of trans-olefins. Chirality. 16: 467-74. PMID 15236344 DOI: 10.1002/chir.20061  1
2004 Solladié-Cavallo A, Roje M, Welter R, Sunji? V. Two-step asymmetric synthesis of disubstituted N-tosyl aziridines having 98-100% ee: use of a phosphazene base. The Journal of Organic Chemistry. 69: 1409-12. PMID 14961706 DOI: 10.1021/jo035586x  1
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  1
2004 Solladié-Cavallo A, Jierry L, Klein A, Schmitt M, Welter R. α-Fluoro decalones as chiral epoxidation catalysts: Fluorine effect Tetrahedron Asymmetry. 15: 3891-3898. DOI: 10.1016/j.tetasy.2004.10.033  1
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  1
2004 Solladié-Cavallo A, Jierry L, Norouzi-Arasi H, Tahmassebi D. Effect of α-fluorination on asymmetric epoxidation of trans-olefins using α-fluorinated cyclohexanone dioxiranes Journal of Fluorine Chemistry. 125: 1371-1377. DOI: 10.1016/j.jfluchem.2004.04.007  1
2004 Šedý O, Solladié-Cavallo A, Sališová M, Bohá? A. Organic phosphazene bases and their utilization in organic chemistry | Organické fosfazénové bázy a ich využitie v organickej chémii Chemicke Listy. 98: 964-969.  1
2003 Solladié-Cavallo A, Marsol C, Yaakoub M, Azyat K, Klein A, Roje M, Suteu C, Freedman TB, Cao X, Nafie LA. erythro-1-Naphthyl-1-(2-piperidyl)methanol: synthesis, resolution, NMR relative configuration, and VCD absolute configuration. The Journal of Organic Chemistry. 68: 7308-15. PMID 12968880 DOI: 10.1021/jo0345502  1
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  1
2003 Solladié-Cavallo A. Organic Chemistry toward Interfaces 3rd Italian-French Meeting on Organic Chemistry, Pisa (Italy) 20-23 November 2002 | Chimie organique aux interfaces 3eRencontre franco-italienne, Pise (Italie) 20-23 novembre 2002 Comptes Rendus Chimie. 6: 515-516. DOI: 10.1016/S1631-0748(03)00093-6  1
2003 Solladié-Cavallo A, Jierry L, Klein A. Asymmetric epoxidation of olefins via new α-fluorinated dioxiranes Comptes Rendus Chimie. 6: 603-606. DOI: 10.1016/S1631-0748(03)00091-2  1
2003 Solladié-Cavallo A, Hoernel F, Schmitt M, Garin F. Heterogeneous asymmetric hydrogenation and deuteration of 2-methyl-2-pentenoic acid over Pd supported catalysts: Proton/deuterium exchange Journal of Molecular Catalysis a: Chemical. 195: 181-188. DOI: 10.1016/S1381-1169(02)00545-9  1
2003 Solladié-Cavallo A, Lupattelli P, Jierry L, Bovicelli P, Angeli F, Antonioletti R, Klein A. Asymmetric oxidation of silyl enol ethers using chiral dioxiranes derived from α-fluoro cyclohexanones Tetrahedron Letters. 44: 6523-6526. DOI: 10.1016/S0040-4039(03)01388-1  1
2003 Solladié-Cavallo A, Lupattelli P, Bonini C, De Bonis M. anti Ethyl β-thienyl-β-amino-α-hydroxy propionate: A regio and stereoselective ring opening of trans ethyl 2-thienyl-glycidate Tetrahedron Letters. 44: 5075-5078. DOI: 10.1016/S0040-4039(03)01127-4  1
2003 Solladié-Cavallo A, Senouci H, Jierry L, Klein A, Bouquey M, Terrisse J. Linseed oil and mixture with maleic anhydride: 1H and 13C NMR Jaocs, Journal of the American Oil Chemists' Society. 80: 311-314.  1
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.  1
2002 Solladié-Cavallo A, Marsol C, Garin F. New chiral modifiers in enantioselective heterogeneous catalytic hydrogenation of ethyl pyruvate over Pt/Al2O3: Chiral amino alcohols derived from piperidine Tetrahedron Letters. 43: 4733-4735. DOI: 10.1016/S0040-4039(02)00936-X  1
2002 Solladié-Cavallo A, Hoernel F, Schmitt M, Garin F. Proton/deuterium exchange in cinchonidine and deuteration of ethyl pyruvate using platinum/Al2O3 catalysts Tetrahedron Letters. 43: 2671-2673. DOI: 10.1016/S0040-4039(02)00400-8  1
2002 Solladié-Cavallo A, Liptaj T, Schmitt M, Solgadi A. iso-Propyl phenylacetate: Formation of a single enolate with tBuP4 as base Tetrahedron Letters. 43: 415-418. DOI: 10.1016/S0040-4039(01)02157-8  1
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.  1
2002 Solladié-Cavallo A, Marsol C, Pescitelli G, Di Bari L, Salvadori P, Huang X, Fujioka N, Berova N, Cao X, Freedman TB, Nafié LA. (R)-(+)- and (S)-(-)-1-(9-phenanthryl)ethylamine: Assignment of absolute configuration by CD tweezer and VCD methods, and difficulties encountered with the CD exciton chirality method European Journal of Organic Chemistry. 1788-1796.  1
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.  1
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  1
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  1
2001 Solladié-Cavallo A, Martin-Cabrejas LM, Caravatti G, Lang M. Synthesis of (+)-(R)-methyl 2-aminotetraline-2-carboxylate: The hydroxypinanone method versus the bislactim method Tetrahedron Asymmetry. 12: 967-969. DOI: 10.1016/S0957-4166(01)00158-6  1
2001 Solladié-Cavallo A, Jierry L, Bouérat L, Taillasson P. Tri- and tetrasubstituted α-fluorocyclohexanones with enantiomeric excesses in the range of 97-100% Tetrahedron Asymmetry. 12: 883-891. DOI: 10.1016/S0957-4166(01)00118-5  1
2001 Solladié-Cavallo A, Marsol C, Hoernel F, Garin F. Substrate-modifier but not catalyst-modifier: Heterogeneous hydrogenation of C=O and C=C using cinchonidine Tetrahedron Letters. 42: 4741-4744. DOI: 10.1016/S0040-4039(01)00838-3  1
2001 Solladié-Cavallo A, Bouérat L, Jierry L. Asymmetric epoxidation of trans-olefins via chiral dioxiranes: A possible contribution of axial approaches in the case of tri- and tetrasubstituted α-fluoro cyclohexanones European Journal of Organic Chemistry. 4557-4560.  1
2001 Solladié-Cavallo A, Marsol C, Suteu C, Garin F. Chromatographic resolution of anthryl- and phenathryl-ethylamines and their use as chiral modifiers for catalytic heterogeneous hydrogenation of ethyl pyruvate Enantiomer. 6: 245-249.  1
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  1
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  1
2000 De Rosa M, Solladié-Cavallo A, Scettri A. A three-step and enantioselective synthesis of (-)-(S)- or (+)-(R)-2- (furan-3-yl)-3,6-dihydro-2H-pyrans Tetrahedron Letters. 41: 1593-1596. DOI: 10.1016/S0040-4039(99)02337-0  1
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.  1
2000 Solladié-Cavallo A, Roje M, Isarno T, Sunjic V, Vinkovic V. Pyridyl and furyl epoxides of more than 99% enantiomeric purities: The use of a phosphazene base European Journal of Organic Chemistry. 1077-1080.  1
1999 Solladié-Cavallo A, Isarno T. Unambiguous and rapid cis/trans assignment of aryl-carboxy disubstituted cyclopropanes using NMR Tetrahedron Letters. 40: 1579-1582. DOI: 10.1016/S0040-4039(98)02649-5  1
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  1
1998 Solladié-Cavallo A, Nsenda T. A four-step synthesis of erythro-m-chloro-3-hydroxytyrosine ethyl ester enantiomerically pure Tetrahedron Letters. 39: 2191-2194. DOI: 10.1016/S0040-4039(98)00172-5  1
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  1
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  1
1998 Nguyên Trong A, Frison G, Solladié-Cavallo A, Metzner P. Some difficulties encountered with AM1 and PM3 calculations Tetrahedron. 54: 12841-12852.  1
1997 Solladié-Cavallo A, Andriamiadanarivo R. Hydroxypinanone: Solute/solute interactions and non-linear chiroptical properties Tetrahedron Letters. 38: 5851-5852. DOI: 10.1016/S0040-4039(97)01301-4  1
1997 Solladié-Cavallo A, Koessler JL, Isarno T, Roche D, Andriamiadanarivo R. The Hydroxypinanone as Chiral Auxiliary in Michael Additions : An Inversion of Diastereoselectivity at Low Concentration of Enolate, a Substrate-Directed Approach Synlett. 1997: 217-218.  1
1996 Solladié-Cavallo A, Roche D, Bold G, Acemoglu F, Tintelnot-Blomley M, Fischer J, De Cian A. Stereoselective synthesis of (4S,5R,6S)-4-(5,6-epoxy-6-phenyl)-γ-lactone Tetrahedron Asymmetry. 7: 1797-1810. DOI: 10.1016/0957-4166(96)00215-7  1
1996 Solladié-Cavallo A, Diep-Vohuule A, Sunjic V, Vinkovic V. A two-step asymmetric synthesis of pure trans-(R,R)-diaryl-epoxides Tetrahedron Asymmetry. 7: 1783-1788. DOI: 10.1016/0957-4166(96)00213-3  1
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  1
1996 Solladié-Cavallo A, Koessler JL, Fischer J, Decian R. Erytftro-selective aldol condensation using directly generated ti-enolates: application to the synthesis of pure ( 1#,2s)-chloramphenicol base and (2r,3r) allo-threonine Gazzetta Chimica Italiana. 126: 173-178.  1
1996 Solladié-Cavallo A, Roche D, Fischer J, De Cian A. Effect of a phosphazene base on the diastereoselectivity of addition of α-sulfonyl carbanions to butyraldehyde and isopropylideneglyceraldehyde Journal of Organic Chemistry. 61: 2690-2694.  1
1995 Solladié-Cavallo A, Diep-Vohuule A. A two-step asymmetric synthesis of (R)-monoaryl epoxides using a chiral oxathiane as a recoverable reagent: Application to the preparation of (R)-β-adrenergic compounds Journal of Organic Chemistry. 60: 3494-3498.  1
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  1
1994 Colonna S, Manfredi A, Solladié-Cavallo A, Quazzotti S, Fischer J, De Cian A. Effect of the nature and position of the chiral auxiliary on stere-oselective synthesis of oxazolines. Rendiconti Lincei. 5: 135-144. DOI: 10.1007/BF03001613  1
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.  1
1994 Solladié-Cavallo A, Csaky AG. Stereochemistry of silyl ketene acetals of some 8-phenylmenthyl arylacetates Journal of Organic Chemistry. 59: 2585-2589.  1
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.  1
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  1
1993 Solladié-Cavallo A, Simon-Wermeister MC, Schwarz J. Diastereoselective monoalkylation of lithium and potassium enolates of a chiral imine of ethyl glycinate: The role of added salts Organometallics. 12: 3743-3747.  1
1992 Solladié-Cavallo A, Quazzotti S, Colonna S, Manfredi A, Fischer J, DeCian A. A three-step synthesis of an enantiomerically pure halostachine analogic starting from η6 (o-tolualdehyde)-chromium-tricarbonyl. Tetrahedron: Asymmetry. 3: 287-296. DOI: 10.1016/S0957-4166(00)80208-6  1
1992 Solladié-Cavallo A, Adib A. Chiral sulfur-reagents for the preparation of optically active epoxides Tetrahedron. 48: 2453-2464. DOI: 10.1016/S0040-4020(01)88764-0  1
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.  1
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.  1
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  1
1991 Solladié-Cavallo A, Khiar N, Fischer J, DeCian A. Configuration and conformation of (-)-8-phenylmenthyl 3-amino-2-hydroxy-5-methylhexanoate Tetrahedron. 47: 249-258. DOI: 10.1016/S0040-4020(01)80921-2  1
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  1
1991 Solladié-Cavallo A, Bencheqroun M. o-Fluorobenzaldehyde-chromium-tricarbonyl: a new chiral complex for highly diastereoselective nucleophilic additions Journal of Organometallic Chemistry. 403: 159-164. DOI: 10.1016/0022-328X(91)83097-N  1
1990 Solladié-Cavallo A, Suffert J, Adib A, Solladié G. A catalytic effect of ZnCl2 during dibal reduction of β-ketosulfoxides. Tetrahedron Letters. 31: 6649-6652. DOI: 10.1016/S0040-4039(00)97137-5  1
1990 Colonna S, Manfredi A, Solladié-Cavallo A, Quazzotti S. Stereoselective synthesis of β-hydroxyamino acids by aldol reaction of α-isocyanocarboxylate with arene-chromium-tricarbonyl complexes. Tetrahedron Letters. 31: 6185-6188. DOI: 10.1016/S0040-4039(00)97020-5  1
1990 Solladié-Cavallo A, Bencheqroun M. N4-isopropyl-N-methyl formamidine, a reagent for the synthesis of bioactive amino-alcohols. Tetrahedron Letters. 31: 2157-2160. DOI: 10.1016/0040-4039(90)80097-6  1
1990 Solladié-Cavallo A, Khiar N. Synthesis of (2S,3R)-3-amino-2-hydroxy-5-methylhexanoic acid: Bridging effect of KF Journal of Organic Chemistry. 55: 4750-4754.  1
1989 Solladié-Cavallo A, Simon MC. Enantioselective synthesis of optically pure natural S(+) or unnatural R(-) DABA Tetrahedron Letters. 30: 6011-6014. DOI: 10.1016/S0040-4039(01)93841-9  1
1989 Bensimon M, Galin JC, Solladié-Cavallo A. Falintolol prodrugs for controlled release. 1. Low molecular weight prodrugs and functionalized monomers through N- and O-regioselective acylation Journal of Controlled Release. 9: 259-270. DOI: 10.1016/0168-3659(89)90095-3  1
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  1
1987 Solladié-Cavallo A, Suffert J. Perfluoroethyl aryl carbinols as inducers of chirality in prelog type syntheses Journal of Fluorine Chemistry. 35: 76-77. DOI: 10.1016/0022-1139(87)95060-3  1
1985 Solladié-Cavallo A. Arene-chromium tricarbonyl complexes: Bonding and behaviour Polyhedron. 4: 901-927. DOI: 10.1016/S0277-5387(00)84058-9  1
1985 Solladié-Cavallo A, Suffert J. Chromium complexed carbinols as highly effective auxiliaries for use in asymmetric induction : reduction of α-ketoesters Tetrahedron Letters. 26: 429-430. DOI: 10.1016/S0040-4039(00)61902-0  1
1983 Solladié-Cavallo A, Haesslein JL. Asymmetric palladium-assisted alkylation of alkenes Helvetica Chimica Acta. 66: 1760-1773. DOI: 10.1002/hlca.19830660615  1
1982 Bäckvall JE, Björkman EE, Byström SE, Solladié-Cavallo A. Palladium-promoted asymetric oxyamination of alkenes application to the synthesis of optically active aryloxypropanolamines Tetrahedron Letters. 23: 943-946. DOI: 10.1016/S0040-4039(00)86989-0  1
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  1
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  1
1982 Solladié-Cavallo A, Suffert J, de Cian A. Some new arene-chromium dicarbonyl chelates Journal of Organometallic Chemistry. 236: 83-93. DOI: 10.1016/S0022-328X(00)86752-2  1
1980 Solladié-Cavallo A, Wipff G. Importance de la conformation des complexes XC6H5Cr(CO)3 pour la regiosélectivité d'additions nucleophiles sur le cycle aromatique Tetrahedron Letters. 21: 3047-3050. DOI: 10.1016/S0040-4039(00)77403-X  1
1978 Solladié-Cavallo A, Solladié G, Tsamo E. Coordination site of Cr(CO)3 in polyaromatic compounds Journal of Organometallic Chemistry. 144: 181-193. DOI: 10.1016/S0022-328X(00)84161-3  1
1976 Olliéro D, Ruxer JM, Solladié-Cavallo A, Solladié G. Optical resolution of a substituted 6,11-diphenyldibenzo[b,f][1,4]diazocine and the racemization barrier Journal of the Chemical Society, Chemical Communications. 276-277. DOI: 10.1039/C39760000276  1
1972 Solladié-Cavallo A, Solladié G. Etude de la stereoselectivite de la quaternarisation de pyrrolidines-1,2 disubstitutees Tetrahedron Letters. 13: 4237-4240. DOI: 10.1016/S0040-4039(01)94284-4  1
1972 Dongala EB, Solladié-Cavallo A, Solladié G. Determination de la purete enantiomerique de β-hydroxyesters partiellement actifs par rmn. Utilisation du tris (trifluoromethylhydroxymethylene)-3 camphorato-d europium III Tetrahedron Letters. 13: 4233-4236. DOI: 10.1016/S0040-4039(01)94283-2  1
1968 Brauman JI, Solladié-Cavallo A. Stereospecific Friedel-Crafts reactions: Alkylation with a cyclic ether Chemical Communications (London). 1124-1125. DOI: 10.1039/C19680001124  1
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