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Tom Boultwood

Department of Chemistry

Imperial College London

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PUBLICATIONS

Highly cis-selective synthesis of iodo-aziridines using diiodomethyllithium and in situ generated N-Boc-imines.

Chemical communications (Cambridge, England) Dec, 2012 | Pubmed ID: 23149421

Palladium-catalyzed cross-coupling of aziridinylmetal species, generated by sulfinyl-magnesium exchange, with aryl bromides: reaction optimization, scope, and kinetic investigations.

The Journal of organic chemistry Feb, 2013 | Pubmed ID: 23311879

Synthesis of cis-C-iodo-N-tosyl-aziridines using diiodomethyllithium: reaction optimization, product scope and stability, and a protocol for selection of stationary phase for chromatography.

The Journal of organic chemistry Jul, 2013 | Pubmed ID: 23738857

Stereospecific Functionalization of Iodoaziridines via Unstabilized Aziridinyllithiums Generated by Iodine-Lithium Exchange.

Organic letters May, 2014 | Pubmed ID: 24786465

INSTITUTIONS

Imperial College London

JOVE ARTICLES

Synthesis and Purification of Iodoaziridines Involving Quantitative Selection of the Optimal Stationary Phase for Chromatography

Tom Boultwood¹,

Dominic P. Affron¹,

James A. Bull¹

¹Department of Chemistry, Imperial College London

Chemistry

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Tom Boultwood

.css-o250i3{font-size:18px;font-family:Open Sans,sans-serif;line-height:21.6px;}Department of Chemistry

Imperial College London

Synthesis and Purification of Iodoaziridines Involving Quantitative Selection of the Optimal Stationary Phase for Chromatography

Department of Chemistry