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Knochel

Submitted by A. Alexakis, G. Cahiez, and J. F. Mormant. Checked by J. Gabriel, P. Knochel, and Dieter Seebach. [Pg.1]

Cunan, D P, P B Jacobs, R. L Elliott, and B H Kim 2 Am Chem Soc. 109, 52SO [19S7j Lowley, M, P D Leeson, B J WlKams, K W Moore, andR Baker Tetralierft-oi , 48,3557 il992 Seebach, D, and P Knochel Hetv Chim Acta. 67, 261 H9S4 ... [Pg.121]

Seebaob, D, and P Knochel Hsiv Chitn. Actti, 69, 261 H9S4 ... [Pg.228]

Knochel et al. described Pd-catalyzed Negishi cross-coupling reactions between zinc organometallics and aryl iodides in [BMMlM][Bp4]. Scheme 5.2-20 illustrates the reaction for the formation of a 3-substituted cyclohexenone from 3-iodo-2-cyclo-hexen-l-one [82]. [Pg.243]

J. Sirieix, M. Ossberger, B. Betze-meier, P. Knochel, Synletters 2000, 1613-1615. [Pg.256]

See Stemmier, T.L. Barnhart, T.M. Penner-Hahn, J.E. Tucker, C.E. Knochel, P. Bohme, M. Frenklng, G. J. Am. Chem. Soc., 1995, 117, 12489 for a discussion concerning the structure of organocuprate reagents. Solution compositions of Gilman reagents have also been studied. See Lipshutz, B.H. Kayser, F. Siegmann, K. Tetrahedron Lett., 1993, 34, 6693. [Pg.650]

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See also in sourсe #XX -- [ Pg.67 ]



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Aldehydes Knochel cuprate addition

Knochel cuprate

Knochel cuprates

Knochel fluorination

Knochel indole synthesis

Knochel procedure

Knochel’s method

Organometallics. Paul Knochel

Paul Knochel, Philip Jones, and Falk Langer ntroduction

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