Arlette Solladié-Cavallo, Ph.D.

École européenne de chimie, polymères et matériaux, University of Strasbourg 
organic chemistry, stereoselective synthesis, NMR
"Arlette Solladié-Cavallo"

Professor Arlette Solladié-Cavallo graduated from Montpellier University (chemistry and physics) in 1961. The same year she earned a Research Engineering degree from Ecole Nationale Supérieures de Chimie de Montpellier (Montpellier, France). She received her PhD degree in 1967 with Professor P. Vièles in the field of physical organic chemistry. After one year as a postdoctoral researcher with Professor J.I. Braumann at Stanford, she returned to Montpellier as a Chargée de Recherches at CNRS (1969). In early seventies she moved to the Ecole Nationale Supérieure de Chimie (Strasbourg, France), which became later Ecole Européenne de Chimie, Polymères et Matériaux (ECPM), a part of the University of Strasbourg. In 1982 she was promoted to Directeur de Recherches at CNRS.

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SOLLADIE-CAVALLO A, BONNE F. (2010) ChemInform Abstract: Synthesis of Enantiomerically Pure threo-1-Alkyl-2- benzyloxypropylamines. Cheminform. 27: no-no
SOLLADIE-CAVALLO A, QUAZZOTTI S. (2010) ChemInform Abstract: An Efficient Synthesis of (+)-8-Phenylmenthyl Isocyanoacetate. Cheminform. 23: no-no
Pažický M, Gášpár B, Solladié-Cavallo A, et al. (2006) 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
Solladié-Cavallo A, Choucair E, Balaz M, et al. (2006) 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
Solladié-Cavallo A, Lupattelli P, Bonini C. (2005) 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
Solladié-Cavallo A, Roje M, Giraud-Roux M, et al. (2004) Trans-diaryl epoxides: asymmetric synthesis, ring-opening, and absolute configuration. Chirality. 16: 196-203
Solladié-Cavallo A, Jierry L, Lupattelli P, et al. (2004) Cyclohexanones derived from dihydrocarvone as precursor of chiral dioxiranes for epoxidation of olefins Tetrahedron. 60: 11375-11381
Solladié-Cavallo A, Balaz M, Salisova M, et al. (2003) New 1,3-oxathianes derived from myrtenal: synthesis and reactivity. The Journal of Organic Chemistry. 68: 6619-26
Solladié-Cavallo A, Balaz M, Salisova M. (2003) Diastereoreactivity of a chiral oxathiane derived from 5-hydroxy-1-tetralone European Journal of Organic Chemistry. 337-345
Solladié-Cavallo A, Lupattelli P, Marsol C, et al. (2002) Opening of diaryl epoxides: Ortho-fluorophenyl and 2-pyridyl epoxides European Journal of Organic Chemistry. 1439-1444
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