Crossref
journal-article
Wiley
Angewandte Chemie International Edition (311)
References
72
Referenced
208
- For reviews see:
10.1002/(SICI)1521-3757(19990802)111:15<2230::AID-ANGE2230>3.0.CO;2-V
10.1002/(SICI)1521-3773(19990802)38:15<2096::AID-ANIE2096>3.0.CO;2-F
10.1002/ejoc.200400751
{'key': 'e_1_2_3_4_2', 'first-page': '2271', 'author': 'Frlan R.', 'year': '2006', 'journal-title': 'Synthesis'}
/ Synthesis by Frlan R. (2006)- See for example:
10.1002/(SICI)1521-3757(19981002)110:19<2868::AID-ANGE2868>3.0.CO;2-3
10.1002/(SICI)1521-3773(19981016)37:19<2704::AID-ANIE2704>3.0.CO;2-1
10.1002/(SICI)1521-3757(19981002)110:19<2872::AID-ANGE2872>3.0.CO;2-0
10.1002/(SICI)1521-3773(19981016)37:19<2708::AID-ANIE2708>3.0.CO;2-E
10.1021/ja030249r
- For selected references see:
10.1021/ja984321a
10.1021/ja990324r
10.1002/ange.200601253
10.1002/anie.200601253
10.1021/ja971901j
10.1039/a805783d
10.1021/ol025839t
10.1021/ol036290g
10.1021/ol062339h
10.1002/chem.200501473
10.1002/adsc.200505385
10.1002/ange.200503538
10.1002/anie.200503538
10.1021/ol0700409
10.1021/ol062904g
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10.1002/adsc.200600628
- For general reviews see:
10.1002/ange.200300594
10.1002/anie.200300594
10.1055/s-2003-42473
10.1016/j.ccr.2004.09.014
10.1021/cr0505268
10.1055/s-2006-939728
- For general reviews see:
10.1021/cr040664h
10.1246/cl.2005.624
- For recent contributions on iron catalysis see:
10.1021/jo0498866
10.1002/ange.200460504
10.1002/anie.200460504
10.1002/ange.200462013
10.1002/anie.200462013
10.1021/ol0523143
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10.1002/anie.200701235
10.1021/ja073084l
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- For selected iron‐catalyzed reactions reported by our group see:
10.1002/ange.200352635
10.1002/anie.200352635
10.1002/ange.200460236
10.1002/anie.200460236
10.1002/adsc.200505163
10.1021/ol060640s
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-
A. Correa C. Bolm Angew. Chem.2007 119 9018–9021;Angew. Chem. Int. Ed.2007 46 8862–8865.
(
10.1002/ange.200703299
) {'key': 'e_1_2_3_56_2', 'first-page': '793', 'volume': '341', 'author': 'Flessner T.', 'year': '1999', 'journal-title': 'J. Prakt. Chem.'}
/ J. Prakt. Chem. by Flessner T. (1999)- When the reaction was performed at lower temperature (110 °C) diphenyl ether (3 a) was obtained in much lower yields.
- All the experiments were carried out with anhydrous FeCl3(purity>98 %) provided by Merck.
- 4‐Nitrophenol has been shown to be unreactive in several copper‐catalyzed O‐arylation reactions with aryl halides. See reference [5g] and references cited therein.
- When using higher catalyst loading (20 mol % FeCl3and 40 mol % L3) no significant improvement was achieved and the corresponding O‐arylated product was obtained in 59 % yield after 20 h.
Dates
Type | When |
---|---|
Created | 17 years, 9 months ago (Dec. 3, 2007, 10:18 a.m.) |
Deposited | 1 year, 10 months ago (Oct. 16, 2023, 8:08 a.m.) |
Indexed | 2 weeks, 3 days ago (Aug. 19, 2025, 6:49 a.m.) |
Issued | 17 years, 8 months ago (Dec. 21, 2007) |
Published | 17 years, 8 months ago (Dec. 21, 2007) |
Published Online | 17 years, 8 months ago (Dec. 21, 2007) |
Published Print | 17 years, 8 months ago (Jan. 4, 2008) |
@article{Bistri_2007, title={Iron‐Catalyzed CO Cross‐Couplings of Phenols with Aryl Iodides}, volume={47}, ISSN={1521-3773}, url={http://dx.doi.org/10.1002/anie.200704018}, DOI={10.1002/anie.200704018}, number={3}, journal={Angewandte Chemie International Edition}, publisher={Wiley}, author={Bistri, Olivia and Correa, Arkaitz and Bolm, Carsten}, year={2007}, month=dec, pages={586–588} }