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Pure Appl. Chem., 1999, Vol. 71, No. 8, pp. 1477-1483

http://dx.doi.org/10.1351/pac199971081477

Selectivity and reactivity in asymmetric allylic alkylation

C. Moberg, Ulf Bremberg, Kristina Hallman, M. Svensson, P.-O. Norrby, Anders Hallberg, Mats Larhed and Ingeborg Csöregh

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  • Moberg Christina, Bremberg Ulf, Hallman Kristina, Svensson Mats, Norrby Per-Ola, Hallberg Anders, Larhed Mats, Csoregh Ingeborg: ChemInform Abstract: Selectivity and Reactivity in Asymmetric Allylic Alkylation. ChemInform 2010, 31, no. <http://dx.doi.org/10.1002/chin.200025301>
  • Foltz Carole, Enders Markus, Bellemin-Laponnaz Stéphane, Wadepohl Hubert, Gade Lutz H.: Using a Tripod as a Chiral Chelating Ligand: Chemical Exchange Between Equivalent Molecular Structures in Palladium Catalysis with 1,1,1-Tris(oxazolinyl)ethane (“Trisox”). Chem Eur J 2007, 13, 5994. <http://dx.doi.org/10.1002/chem.200700307>
  • Hu Libo, Wang Yikai, Li Bonan, Du Da-Ming, Xu Jiaxi: Diastereoselectivity in the Staudinger reaction: a useful probe for investigation of nonthermal microwave effects. Tetrahedron 2007, 63, 9387. <http://dx.doi.org/10.1016/j.tet.2007.06.112>
  • Maezaki Naoyoshi, Yano Masahiro, Hirose Yuki, Itoh Yoshikazu, Tanaka Tetsuaki: Stereodivergent synthesis of 1,4-bifunctional compounds by regio- and diastereoselective Pd-catalyzed allylic substitution reaction. Tetrahedron 2006, 62, 10361. <http://dx.doi.org/10.1016/j.tet.2006.08.057>
  • Thienthong Neeranat, Perlmutter Patrick: A new class of nitrogen based chiral ligands: 2H-1,3-benzoxazines. Ligand synthesis, X-ray structural studies and asymmetric catalysis. J Organomet Chem 2005, 690, 2027. <http://dx.doi.org/10.1016/j.jorganchem.2004.11.047>
  • Dong Ying, Teesdale-Spittle Paul, Hoberg John O.: Regioselective palladium-catalyzed allylic alkylations. Tetrahetron Lett 2005, 46, 353. <http://dx.doi.org/10.1016/j.tetlet.2004.09.190>
  • Lidström Pelle, Tierney Jason, Wathey Bernard, Westman Jacob: Microwave assisted organic synthesis—a review. Tetrahedron 2001, 57, 9225. <http://dx.doi.org/10.1016/S0040-4020(01)00906-1>