scholarly journals A facile preparation of 4-aryl-3-[(tert-butyldimethylsilyl)oxymethyl]furans

1991 ◽  
Vol 69 (8) ◽  
pp. 1326-1330 ◽  
Author(s):  
Brian A. Keay ◽  
Jean-Louis J. Bontront

A series of aryl bromides undergo a palladium-catalyzed coupling reaction with 3-[(tert-butyldimethylsilyl)oxymethyl]-4-(tri-n-butylstannyl)furan to provide 4-aryl-3-[(tert-butyldimethylsilyl)oxymethyl]furans in moderate to good yields. Key words: palladium, cross-couplings, stannanes, 3,4-disubstituted furans.

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 ◽  
2001 ◽  
Vol 2001 (15) ◽  
pp. 2231-2233 ◽  
Author(s):  
Miki Murata ◽  
Ryuta Shimazaki ◽  
Shinji Watanabe ◽  
Yuzuru Masuda

1998 ◽  
Vol 39 (26) ◽  
pp. 4673-4676 ◽  
Author(s):  
Jun-Ichi Inoh ◽  
Tetsuya Satoh ◽  
Sommai Pivsa-Art ◽  
Masahiro Miura ◽  
Masakatsu Nomura

Synlett ◽  
2017 ◽  
Vol 28 (20) ◽  
pp. 2812-2816 ◽  
Author(s):  
Fumiki Ichioka ◽  
Yuhei Itai ◽  
Yuji Nishii ◽  
Masahiro Miura

Direct coupling reaction of benzo[b]thiophene and electron-rich aryl bromides was achieved under Pd2(dba)3/SPhos catalysis in the presence of NaOt-Bu. The reaction system was applied for the installation of 2-(methylthio)phenyl group onto thiophene-fused polyaromatic molecules, demonstrating facile synthesis of precursors for thienoacene derivatives.


Synlett ◽  
1995 ◽  
Vol 1995 (12) ◽  
pp. 1225-1226 ◽  
Author(s):  
Hiroshi Oda ◽  
Katsuaki Hamataka ◽  
Keigo Fugami ◽  
Masanori Kosugi ◽  
Toshihiko Migita

ChemInform ◽  
2012 ◽  
Vol 43 (30) ◽  
pp. no-no
Author(s):  
Fangfang Ma ◽  
Xiaomin Xie ◽  
Lina Ding ◽  
Jinsheng Gao ◽  
Zhaoguo Zhang

Sign in / Sign up

Export Citation Format

Share Document