ChemInform Abstract: SELECTIVE MONO-ALKYLATION AND ARYLATION OF AROMATIC DIHALIDES BY PALLADIUM-CATALYZED CROSS-COUPLING WITH THE GRIGNARD AND ORGANOZINC REAGENTS

1980 ◽  
Vol 11 (23) ◽  
Author(s):  
A. MINATO ◽  
K. TAMAO ◽  
T. HAYASHI ◽  
K. SUZUKI ◽  
M. KUMADA
2002 ◽  
Vol 67 (11) ◽  
pp. 1658-1668 ◽  
Author(s):  
Agnieszka Przezdziecka ◽  
Alicja Kurek-Tyrlik ◽  
Jerzy Wicha

Palladium-catalyzed coupling of steroid 17-iodo-6β-methoxy-3α,5-cyclo-5α-androst-16-ene (4) 17-iodoandrosta-5,16-dien-3β-ol (5), and structurally similar (3aS,7R,7aR)-benzenesulfonyl-3-iodo-3a-methyl-3a,4,5,6,7,7a-hexahydro-1H-indene (6) with various arylzinc chlorides, which were generated from aryl bromides 8 [1-bromomethylbenzene (8a), O-(triethylsilyl-2-bromophenyl)propan-2-ol (8b), 2-(4-bromophenyl)propan-2-ol (8c), 4-bromobenzonitrile (8d), 4-bromobenzoic acid methyl ester (8e), 4-bromobenzoic acid tert-butyl ester (8f) and 3-bromopyridine (8g)] via aryllihium derivatives (the Negishi coupling) was examined. The respective cross-coupling products were obtained in good yields for all aryl bromides except of 8c and 8e. Building blocks for synthesis of certain vitamin D analogues have been prepared.


Synthesis ◽  
2010 ◽  
Vol 2010 (12) ◽  
pp. 2085-2091 ◽  
Author(s):  
Paul Knochel ◽  
Laurin Melzig ◽  
Jérémy Stemper

1980 ◽  
Vol 21 (9) ◽  
pp. 845-848 ◽  
Author(s):  
Akio Minato ◽  
Kohei Tamao ◽  
Tamio Hayashi ◽  
Keizo Suzuki ◽  
Makoto Kumada

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