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For examples of transition metal-catalyzed hydroarylation/lactonization using alkynoates and arylboronic acids, see:
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For examples of transition metal-catalyzed hydroarylation/lactonization using alkynoates and arylboronic acids, see:. Oh C.H., Park S.J., Ryu J.H., and Kumar Gupta A. Tetrahedron Lett. 45 (2004) 7039
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For examples of transition metal-catalyzed hydroarylation/lactonization using alkynoates and aryl halides and congeners, see:
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For examples of transition metal-catalyzed hydroarylation/lactonization using alkynoates and aryl halides and congeners, see:. Arcadi A., Bernocchi E., Burini A., Cacchi S., Marinelli F., and Pietroni B. Tetrahedron 44 (1988) 481
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15
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4944233291
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Palladium-catalyzed 2:2 coupling of diarylalkynes and arylboronic acids has been reported, see:
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Palladium-catalyzed 2:2 coupling of diarylalkynes and arylboronic acids has been reported, see:. Satoh T., Ogino S., Miura M., and Nomura M. Angew. Chem. Int. Ed. 43 (2004) 5063
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17
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76949108404
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Oligobutenlides were obtained from the Rh-catalyzed hydroarylation of ethyl 4-hydroxy-4-dimethyl-2-pentynoate with phenylboron reagents, see ref 5b
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Oligobutenlides were obtained from the Rh-catalyzed hydroarylation of ethyl 4-hydroxy-4-dimethyl-2-pentynoate with phenylboron reagents, see ref 5b.
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23
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Taniguchi T., Nagata H., Kanada R.M., Kadota K., Tekeuchi M., and Ogasawara K. Heterocycles 52 (2000) 67
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Ogasawara, K.6
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