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For three-component coupling using trimethylsilyltributylstannane instead of silane, see:
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For reviews on Ni(0)-catalyzed multicomponent coupling, see:
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For recent examples of Ni(0)-catalyzed multicomponent coupling, see:
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For recent examples of Ni(0)-catalyzed multicomponent coupling, see:. Mahandru G.M., Liu G., and Montgomery J. J. Am. Chem. Soc. 126 (2004) 3698-3699
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For Ni-catalyzed reductive coupling of 1,3-diene and aldehyde using organometallic reagent in the absence or in the presence of phosphine ligand, see:
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For Ni-catalyzed reductive coupling of 1,3-diene and aldehyde using organometallic reagent in the absence or in the presence of phosphine ligand, see:. Kimura M., Ezoe A., Shibata K., and Tamaru Y. J. Am. Chem. Soc. 120 (1998) 4033-4034
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0033570981
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For a pioneering work on Ni-catalyzed alkylative coupling of 1,3-dienes and aldehydes, see:
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For a pioneering work on Ni-catalyzed alkylative coupling of 1,3-dienes and aldehydes, see:. Kimura M., Matsuo S., Shibata K., and Tamaru Y. Angew. Chem., Int. Ed. 38 (1999) 3386-3388
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0345831185
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For an intramolecular alkylative cyclization of 1,3-diene and aldehyde using Ni catalyst, see:
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For an intramolecular alkylative cyclization of 1,3-diene and aldehyde using Ni catalyst, see:. Sato Y., Takanashi T., and Mori M. Organometallics 18 (1999) 4891-4893
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30
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46749128198
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note
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For details of the determination of the relative configuration of the coupling products, see Supplementary data.
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-
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31
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46749132358
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note
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3 or PhB(pin)) or that in other solvents (1,4-dioxane, toluene, DMF, DMSO, or MeCN) gave poor results.
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-
-
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32
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2042507954
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3 is indispensable for the Ni-catalyzed three-component coupling is not clear yet, the base would activate organoboronic acids as in the case of Miyaura-Suzuki reaction. For reviews on the Miyaura-Suzuki reaction, see:
-
3 is indispensable for the Ni-catalyzed three-component coupling is not clear yet, the base would activate organoboronic acids as in the case of Miyaura-Suzuki reaction. For reviews on the Miyaura-Suzuki reaction, see:. Miyaura N., and Suzuki A. Chem. Rev. 95 (1995) 2457-2483
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Suzuki A. In: Negishi E.-i., and de Meijere A. (Eds). Handbook of Organopalladium Chemistry of Organic Synthesis Vol. I (2002), Wiley-Interscience, A John Wiley & Sons, New York 249-262
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Suzuki, A.1
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84891341770
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For recent review on Ni-catalyzed cross-coupling including Miyaura-Suzuki type reaction, see:. Tamaru Y. (Ed), Wiley-VCH GmbH & Co. KGaA, Weinheim
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For recent review on Ni-catalyzed cross-coupling including Miyaura-Suzuki type reaction, see:. Takahashi T., and Kanno K.-i. In: Tamaru Y. (Ed). Modern Organonickel Chemistry (2005), Wiley-VCH GmbH & Co. KGaA, Weinheim 41-55
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3-allylalkoxynickel complex from 1,3-diene and aldehyde in the presence of tricyclohexylphosphine ligand was isolated and the structure was elucidated by X-ray analysis:
-
3-allylalkoxynickel complex from 1,3-diene and aldehyde in the presence of tricyclohexylphosphine ligand was isolated and the structure was elucidated by X-ray analysis:. Ogoshi S., Tonomori K.-i., Oka M.-a., and Kurosawa H. J. Am. Chem. Soc. 128 (2006) 7077-7086
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