DOI: 10.1002/anie.200301760. Organocatalyzed Asymmetric α‐Aminoxylation of Aldehydes and Ketones—An Efficient Access to Enantiomerically Pure α‐Hydroxycarbonyl Compounds, Diols, and Even Amino Alcohols

Organocatalyzed Asymmetric α‐Aminoxylation of Aldehydes and Ketones—An Efficient Access to Enantiomerically Pure α‐Hydroxycarbonyl Compounds, Diols, and Even Amino Alcohols

10.1002/anie.200301760

Crossref journal-article

Wiley

Angewandte Chemie International Edition (311)

Bibliography

Merino, P., & Tejero, T. (2004). Organocatalyzed Asymmetric Î±âAminoxylation of Aldehydes and KetonesâAn Efficient Access to Enantiomerically Pure Î±âHydroxycarbonyl Compounds, Diols, and Even Amino Alcohols. Angewandte Chemie International Edition, 43(23), 2995â2997. Portico.

Authors 2

Pedro Merino (first)
Tomas Tejero (additional)

References 38 Referenced 183

{'key': 'e_1_2_2_1_2', 'volume-title': 'Organic Synthesis', 'author': 'Fuhrhop J.', 'year': '1994'} / Organic Synthesis by Fuhrhop J. (1994)
{'key': 'e_1_2_2_2_2', 'first-page': '4497', 'volume-title': 'Houben Weyl: Methods of Organic Chemistry. Stereoselective Synthesis, Vol. E21', 'author': 'Davis F. A.', 'year': '1996'} / Houben Weyl: Methods of Organic Chemistry. Stereoselective Synthesis, Vol. E21 by Davis F. A. (1996)
10.1021/cr00013a008
10.1021/ar980062i
10.2174/1385272003376210
Special Issue on Enantioselective Synthesis:Chem. Rev.2003 103(8) 2761–3400. (10.1021/cr030693c)
10.1021/ja9726668
10.1016/0040-4039(88)85224-9
{'key': 'e_1_2_2_11_2', 'volume-title': 'Asymmetric Oxidation Reactions', 'author': 'Zhou P.', 'year': '2001'} / Asymmetric Oxidation Reactions by Zhou P. (2001)
10.1002/ange.200390228
10.1002/anie.200390283
For reviews on nitroso compounds see:
10.1021/cr00030a007
10.1021/cr0000731
10.1021/ol026443k
10.1002/1521-3757(20020816)114:16<3112::AID-ANGE3112>3.0.CO;2-N
10.1002/1521-3773(20020816)41:16<2986::AID-ANIE2986>3.0.CO;2-F
10.1021/ja0298702
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10.1002/1521-3773(20011015)40:20<3726::AID-ANIE3726>3.0.CO;2-D
10.1055/s-2001-18074
10.1126/science.1076547
10.1016/S0040-4020(02)00516-1
10.1021/ja037096s
10.1016/j.tetlet.2003.09.057
10.1002/ange.200352097
10.1002/anie.200352097
In fact most experiments carried out by Hayashi and co‐workers (see ref. [18]) are conducted in the presence of 30 mol % (S)‐proline. Similarly Zhong (see ref. [19]) used 20 mol % catalyst.
10.1002/ange.200353018
10.1002/anie.200353018
10.1002/ange.200353085
10.1002/anie.200353085
10.1126/science.287.5460.1964
10.1002/ange.200300626
10.1002/anie.200300626

Dates

Type	When
Created	21 years, 3 months ago (May 13, 2004, 11:04 a.m.)
Deposited	1 year, 10 months ago (Oct. 10, 2023, 11:50 a.m.)
Indexed	2 days, 4 hours ago (Sept. 4, 2025, 10 a.m.)
Issued	21 years, 3 months ago (June 1, 2004)
Published	21 years, 3 months ago (June 1, 2004)
Published Online	21 years, 3 months ago (June 1, 2004)
Published Print	21 years, 2 months ago (June 7, 2004)

Funders 0

None

BibTeX

@article{Merino_2004, title={Organocatalyzed Asymmetric α‐Aminoxylation of Aldehydes and Ketones—An Efficient Access to Enantiomerically Pure α‐Hydroxycarbonyl Compounds, Diols, and Even Amino Alcohols}, volume={43}, ISSN={1521-3773}, url={http://dx.doi.org/10.1002/anie.200301760}, DOI={10.1002/anie.200301760}, number={23}, journal={Angewandte Chemie International Edition}, publisher={Wiley}, author={Merino, Pedro and Tejero, Tomas}, year={2004}, month=jun, pages={2995–2997} }

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