И снова я прошу о помощи.
1. Aillaud, Isabelle; Wright, Karen; Collin, Jacqueline; Schulz, Emmanuelle; Mazaleyrat, Jean-Paul; New axially chiral atropos and tropos secondary diamines as ligands for enantioselective intramolecular hydroamination. Tetrahedron: Asymmetry; English; 19; 1; 2008; 82 - 92;
Код: Выделить всё
http://dx.doi.org/10.1016/j.tetasy.2007.11.029
2. Liu, Xu-Guang; Jiang, Jia-Jun; Shi, Min; Development of axially chiral bis(arylthiourea)-based organocatalysts and their application in the enantioselective Henry reaction. Tetrahedron: Asymmetry; English; 18; 23; 2007; 2773 -2781;
Код: Выделить всё
http://dx.doi.org/10.1016/j.tetasy.2007.11.008
3. Guillena, Gabriela; Hita, Maria del Carmen; Najera, Carmen; Viozquez, Santiago F.; Solvent-free asymmetric direct aldol reactions organocatalysed by recoverable (Sa)-binam-l-prolinamide. Tetrahedron: Asymmetry; English; 18; 19; 2007; 2300 - 2304;
Код: Выделить всё
http://dx.doi.org/10.1016/j.tetasy.2007.09.020
4. Guizzetti, Stefania; Benaglia, Maurizio;Pignataro, Luca; Puglisi, Alessandra; A multifunctional proline-based organic catalyst for enantioselective aldol reactions. Tetrahedron:Asymmetry; English; 17; 19; 2006; 2754 - 2760;
Код: Выделить всё
http://dx.doi.org/10.1016/j.tetasy.2006.10.018
5. Guillena, Gabriela; Hita, Maria del Carmen; Najera, Carmen; BINAM-prolinamides as recoverable catalysts in the direct aldol condensation. Tetrahedron: Asymmetry; English; 17;5; 2006; 729 - 733;
Код: Выделить всё
http://dx.doi.org/10.1016/j.tetasy.2006.02.004
6. Gaeta, Carmine; Rosa, Margherita De; Fruilo,Marina; Soriente, Annunziata; Neri, Placido; Synthesis of calix[4]arene derivatives bearing chiral pendant groups as ligands for enantioselective catalysis. Tetrahedron: Asymmetry; English; 16; 13; 2005; 2333 - 2340;
Код: Выделить всё
http://dx.doi.org/10.1016/j.tetasy.2005.05.039
7. Johansson, Magnus J.; Schwartz, Lennart; Amedjkouh, Mohamed; Kann, Nina; New chiral amine ligands in the desymmetrization of prochiral phosphine boranes. Tetrahedron:Asymmetry; English; 15; 22; 2004; 3531 - 3538;
Код: Выделить всё
http://dx.doi.org/10.1016/j.tetasy.2004.09.023
8. Yus, Miguel; Ramon, Diego J.; Prieto, Oscar; Synthesis of new C2-symmetrical bis(hydroxycamphorsulfonamide) ligands and their application in the enantioselective addition of dialkylzinc reagents to aldehydes and ketones. Tetrahedron: Asymmetry; English; 14; 9; 2003; 1103 -1114;
Код: Выделить всё
http://dx.doi.org/10.1016/S0957-4166(03)00045-4
9. Shi, Min; Wang, Chun-Jiang; Axially dissymmetric binaphthyldiimine chiral Salen-type ligands for catalytic asymmetric addition of diethylzinc to aldehyde. Tetrahedron: Asymmetry; English; 13; 19; 2002; 2161 - 2166;
Код: Выделить всё
http://dx.doi.org/10.1016/S0957-4166(02)00571-2
10. Shi, Min; Wang, Chuan-Jiang; Chan, Albert S. C.; Axially dissymmetric binaphthyldiimine chiral salen-type ligands for copper-catalyzed asymmetric aziridination. Tetrahedron: Asymmetry; English; 12; 22; 2001;3105 - 3112;
Код: Выделить всё
http://dx.doi.org/10.1016/S0957-4166(01)00534-1
11. Quirmbach, Michael Kless, Achim; Holz, Jens;Tararov, Vitali; Boerner, Armin; Construction of chiral Ti(IV)–Rh(I)–salenophos complexes and their application in the asymmetric hydroformylation of functionalised olefins. Tetrahedron:Asymmetry; English; 10; 9; 1999; 1803 - 1812;
Код: Выделить всё
http://dx.doi.org/10.1016/S0957-4166(99)00165-2
12. Nozaki, Kyoko; Terakawa, Takakiyo; Takaya, Hidemasa; Hiyama, Tamejiro; Cyclic polyamides consisting of 1,1′-binaphthyls. ‘Chiral twist’ of glycine residues. Tetrahedron: Asymmetry; English; 8; 20; 1997; 3431 - 3436;
Код: Выделить всё
http://dx.doi.org/10.1016/S0957-4166(97)00460-6
13. Adolfsson, Hans; Moberg, Christina; Chiral lewis acid catalysed asymmetric nucleophilic ring opening of cyclohexene oxide. Tetrahedron: Asymmetry; English; 6; 8; 1995; 2023 - 2032;
Код: Выделить всё
http://dx.doi.org/10.1016/0957-4166(95)00263-O
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