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Transition metal organometallics in organic synthesis
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(Eds.: E. W. Able, F. G. A. Stone, G. Willkinson), Pergamon, Oxford
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(Eds.: E. W. Able, F. G. A. Stone, G. Willkinson), Pergamon, Oxford
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a) "Transition Metal Alkyne Complexes: Zirconium - Benzyne Complexes": S. L. Buchwald, R. D. Broene in Comprehensive Organometallic Chemistry II, Vol. 12 (Eds.: E. W. Able, F. G. A. Stone, G. Willkinson), Pergamon, Oxford, 1995, pp. 771-784;
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Transition metal allyl complexes: Intermolecular alkene and alkyne insertion
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(Eds.: E. W. Able, F. G. A. Stone, G. Willkinson), Pergamon, Oxford
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a) "Transition Metal Allyl Complexes: Intermolecular Alkene and Alkyne Insertion": W. Oppolzer, in Comprehensive Organometallic Chemistry II, Vol. 12 (Eds.: E. W. Able, F. G. A. Stone, G. Willkinson), Pergamon, Oxford, 1995, pp. 905-921;
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The insertion reaction of alkynes into π-allyl nickel complexes is known: a) F. Camps, J. M. Moretó, L. Pagès, Tetrahedron 1992, 48, 3147-3162;
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b) J. Montgomery, E. Oblinger, A. V. Savchenko, J. Am. Chem. Soc. 1997, 119, 4911-4920;
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25
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0343399606
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note
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Significant amounts of triphenylene (20-30%) were produced as a by-product in Method B (entry 2), but only a trace amount of it was detected in Method A (entry 1).
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0343399605
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note
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2 unit.
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0343399604
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note
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3CN (1 mL) and THF (1 mL) was treated with 1 (0.4 mmol) at 60 C for 1 day. Further CsF (0.8 mmol) was then added and the resulting mixture was st irred at 60 C for 1 day.
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