Swern oxidation


Definition: The oxidation of a primary alcohol or secondary alcohol to an aldehyde or ketone respectively. Does not work with allylic or benzylic alcohols.

ID: RXNO:0000154

More about the RSC Name Reaction Ontology (RXNO)


Articles referencing this term

Total syntheses of (±)-montanin A and (±)-teuscorolide
I-Chia Chen, Yen-Ku Wu, Hsing-Jang Liu and Jiang-Liang Zhu, Chem. Commun., 2008 , 4720
DOI: 10.1039/b807218c

Chemistry and structural determination of botcinolides, botcinins, and botcinic acids
Isamu Shiina and Hiroki Fukui, Chem. Commun., 2009 , 385
DOI: 10.1039/b814375g

Iterative synthesis of acenes via homo-elongation
Chih-Hsiu Lin, Ke-Han Lin, Bikash Pal and Li-Der Tsou, Chem. Commun., 2009 , 803
DOI: 10.1039/b814840f

Highly regioselective ring-opening of trisubstituted aziridines by sulfur-stabilised carbanions
Santiago Carballares, Donald Craig, Christopher J. T. Hyland, Pengfei Lu, Tanya Mathie and Andrew J. P. White, Chem. Commun., 2009 , 451
DOI: 10.1039/b815971h

Total synthesis of (−)-spirangien A and its methyl ester
Ian Paterson, Alison D. Findlay and Christian Noti, Chem. Commun., 2008 , 6408
DOI: 10.1039/b816229h

The asymmetric total synthesis of (−)-securinine
Bhartesh Dhudshia, Benjamin F. T. Cooper, Charles L. B. Macdonald and Avinash N. Thadani, Chem. Commun., 2009 , 463
DOI: 10.1039/b816576a

An enantiopure cyclophane-type imidazole with no central but planar chirality
Yasuhiro Ishida, Eriko Iwasa, Yuki Matsuoka, Hiroyuki Miyauchi and Kazuhiko Saigo, Chem. Commun., 2009 , 3401
DOI: 10.1039/b904059e

Intramolecular aryl transfer to thionium ions in an approach to α-arylacetamides
Caroline Ovens, Johannes C. Vogel, Nathaniel G. Martin and David J. Procter, Chem. Commun., 2009 , 3101
DOI: 10.1039/b904577e

A three-step tandem process for the synthesis of bicyclic γ-lactams
Fiona I. McGonagle, Lindsay Brown, Andrew Cooke and Andrew Sutherland, Org. Biomol. Chem., 2010 , 8 , 3418
DOI: 10.1039/c004695g

Synthesis and NMDA receptor affinity of dexoxadrol analogues with modifications in position 4 of the piperidine ring
Ashutosh Banerjee, Roland Fröhlich, Dirk Schepmann and Bernhard Wünsch, Med. Chem. Commun., 2010 , 1 , 87
DOI: 10.1039/c0md00017e

Stereoselective synthesis of epi-jasmonic acid, tuberonic acid, and 12-oxo-PDA
Hisato Nonaka, Narihito Ogawa, Noriaki Maeda, Yong-Gang Wang and Yuichi Kobayashi, Org. Biomol. Chem., 2010 , 8 , 5212
DOI: 10.1039/c0ob00218f

Stereoselective synthesis of the bicyclic guanidine alkaloid (+)-monanchorin
Ahmed M. Zaed and Andrew Sutherland, Org. Biomol. Chem., 2010 , 8 , 4394
DOI: 10.1039/c0ob00219d