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Pure Appl. Chem., 1988, Vol. 60, No. 11, pp. 1607-1614

http://dx.doi.org/10.1351/pac198860111607

Asymmetric C-C bond formation using organometallic chemistry

M. T. Reetz

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  • Bhakta Urmibhusan, Sullivan Erin, Hall Dennis G.: Catalytic enantioselective allylboration of propargylic aldehydes. Tetrahedron 2014, 70, 678. <http://dx.doi.org/10.1016/j.tet.2013.11.095>
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  • Bower John F., Kim In Su, Patman Ryan L., Krische Michael J.: Katalytische Carbonyladdition durch Transferhydrierung: weg von vorab gebildeten Organometallreagentien. Angew. Chem. 2009, 121, 36. <http://dx.doi.org/10.1002/ange.200802938>
  • Bower John F., Kim In Su, Patman Ryan L., Krische Michael J.: Catalytic Carbonyl Addition through Transfer Hydrogenation: A Departure from Preformed Organometallic Reagents. Angew. Chem. Int. Ed. 2009, 48, 34. <http://dx.doi.org/10.1002/anie.200802938>
  • Denmark Scott E., Collins William R., Cullen Matthew D.: Observation of Direct Sulfenium and Selenenium Group Transfer from Thiiranium and Seleniranium Ions to Alkenes. J Am Chem Soc 2009, 131, 3490. <http://dx.doi.org/10.1021/ja900187y>
  • Kim In Su, Krische Michael J., Han Soo Bong: Enantioselective iridium-catalyzed carbonyl allylation from the alcohol oxidation level via transfer hydrogenation: minimizing pre-activation for synthetic efficiency. Chem Commun 2009, 7278. <http://dx.doi.org/10.1039/b917243m>
  • Lutz Christian, Lutz Volker, Knochel Paul: Enantioselective synthesis of 1,2-, 1,3- and 1,4- aminoalcohols by the addition of dialkylzincs to 1,2-, 1,3- and 1,4- aminoaldehydes. Tetrahedron 1998, 54, 6385. <http://dx.doi.org/10.1016/S0040-4020(98)00297-X>
  • Wilken Jörg, Thorey Claire, Gröger Harald, Haase Detlev, Saak Wolfgang, Pohl Siegfried, Muzart Jacques, Martens Jürgen: Utilization of Industrial Waste Materials, 11. Synthesis of New, Chiral β-sec-Amino Alcohols – Diastereodivergent Addition of Grignard Reagents to α-Amino Aldehydes Based on the (all-R)-2-Azabicyclo[3.3.0]octane System. Liebigs Ann /Recueil 1997, 1997, 2133. <http://dx.doi.org/10.1002/jlac.199719971016>
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  • Mears Richard J., De Silva Harshani, Whiting Andrew: Synthesis of a new C2-symmetric chiral diol: Application to asymmetric allylboration. Tetrahedron 1997, 53, 17395. <http://dx.doi.org/10.1016/S0040-4020(97)10163-6>
  • Fussing Ingrid M.M., Pletcher Derek, Whitby Richard J.: The synthesis and electrochemistry of CpTiCl2(OR) (R = alkyl, aryl) complexes. J Organomet Chem 1994, 470, 109. <http://dx.doi.org/10.1016/0022-328X(94)80154-1>
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  • Frenking G., Köhler K.F., Reetz M.T.: On the origin of π-facial diastereoselectivity in nucleophilic additions to chiral carbonyl compounds 3. Rotational profiles of 2-methoxypropanal and 2-N,N-dimethylaminopropanal. Tetrahedron 1993, 49, 3971. <http://dx.doi.org/10.1016/S0040-4020(01)89911-7>
  • Reetz Manfred T., Jaeger Ralf, Drewlies Ralf, Hübel Marcus: Stereoselektive Synthese von vicinalen Diaminen. Angew Chem 1991, 103, 76. <http://dx.doi.org/10.1002/ange.19911030111>
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  • Reetz M.T., Lauterbach E.H.: Stereoselective epoxidation of chiral electron-poor γ-aminoolefins. Tetrahetron Lett 1991, 32, 4477. <http://dx.doi.org/10.1016/0040-4039(91)80016-Y>
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  • Frenking G, Köhler K.F, Reetz M.T: On the origin of π-facial diastereoselectivity in nucleophilic additions to chiral carbonyl compounds. 1. Rotational profiles of propionaldehyde 1, chloroacetaldehyde 2, and 2-chloropropionaldehyde 3. Tetrahedron 1991, 47, 8991. <http://dx.doi.org/10.1016/S0040-4020(01)86504-2>
  • Brückner Reinhard, Harms Klaus, Priepke Henning: Asymmetric Induction in the Wittig-Still Rearrangement of Ethers Containing an Allylic Stereocenter – Diastereocontrol by Allylic Nitrogen. Chem Ber 1990, 123, 555. <http://dx.doi.org/10.1002/cber.19901230323>
  • Duthaler Rudolf O., Herold Peter, Wyler-Helfer Susanne, Riediker Martin: Enantio- and Diastereoselective Aldol-Reaction of 2,6-Dimethylphenyl Propionate Using Titanium-Carbohydrate Complexes. HCA 1990, 73, 659. <http://dx.doi.org/10.1002/hlca.19900730315>
  • Jako Isabelle, Uibera Pierre, Mann André, Taddei Maurizio, Wermuth Camille-Georges: Diastereoselectivity in conjugate addition of alkylcuprates to vinylogous ester of N O-diprotected serinal. Tetrahetron Lett 1990, 31, 1011. <http://dx.doi.org/10.1016/S0040-4039(00)94416-2>
  • Reetz M.T., Rivadeneira E., Niemeyer C.: Reagent control in the aldol addition of chiral boron enolates based on the 2,5-diphenylborolane ligand system. Tetrahetron Lett 1990, 31, 3863. <http://dx.doi.org/10.1016/S0040-4039(00)97489-6>
  • Vara Prasad J.V.N., Rich Daniel H.: Addition of Allylic Metals to α-Aminoaldehydes. Application to the Synthesis of Statine, Ketomethylene and Hydroxyethylene Dipeptide Isosteres. Tetrahetron Lett 1990, 31, 1803. <http://dx.doi.org/10.1016/S0040-4039(00)98790-2>
  • Reetz M.T., Schmitz A., Holdgrün X.: Tandem aldolization/lactonization/dyotropic rearrangement of α-amino-aldehydes. Tetrahetron Lett 1989, 30, 5421. <http://dx.doi.org/10.1016/S0040-4039(01)80583-9>
  • Reetz M.T., Binder J.: Protective group tuning in the stereoselective conversion of α-amino aldehydes into aminoalkyl epoxides. Tetrahetron Lett 1989, 30, 5425. <http://dx.doi.org/10.1016/S0040-4039(01)80584-0>