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1. (a) Hoppe, D.; Hintze, F.; Tebben, P. Angew. Chem. 1990, 102, 1457-1459; Angew. Chem. Int. Ed. Engl. 1990, 29, 1422-1423;
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2. (a) First example: Drozd, V. N.; Ustynyuk, U. A.; Tsel'eva, M. A.; Dmitriev, L. B. J. Gen. Chem. USSR 1968, 38, 2047; Zh. Obsch. Khim. 1968, 38, 2114;
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(e) Krief, A.; Kenda, B.; Barbeaux, P.; Guittet, E. ibid. 1994, 50, 7177-7192;
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5. Example of an enantioselective intermolecular carbolithiation: Klein, S.; Marek, I.; Poisson, J.-F.; Normant, J.-F. J. Am. Chem. Soc. 1995, 777, 8853-8854.
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Sonogashira, K.1
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0010561621
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note
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(b) The enantioselective reduction with (S)-Alpine-Borane® and (R)-Alpine-Borane® gives the (S)-and the (R)-configurated secondary alkanol, respectively.
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10. (a) Dale, J. A.; Dull, D. L.; Mosher, H. S. J. Org. Chem. 1969, 34, 2543-2549;
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Dale, J.A.1
Dull, D.L.2
Mosher, H.S.3
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0010561479
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note
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19F-NMR.
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0010595960
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note
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3);
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0010628598
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note
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(b) All isolated compounds gave satisfactory analytical and spectroscopic data.
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0010630792
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note
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12. Crystal structure data of cis-15a: Crystallographic data (excluding structure factors) for the structures reported in this paper have been deposited with the Cambridge Crystallographic Data Centre.
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