Abmacr Reaction of 1-(%racrlylmethylene)pyndtmum salts wtth tb~ols leads to the formauon of the comqondmg thymme denvauves This transformatmn of a urzd dertvahve to the correqondmg thymme IS explamed on the basis of the formauon of an exccycbcmethylene mtenuedmte, analogous to that proposed m the th
✦ LIBER ✦
Reduction of 1-(5-uracilylmethyl)pyridinium salts by thiols to thymine derivatives. A model of the thymidylate synthase reaction
✍ Scribed by Erwin Vega; Eduard R. de Waard; Upendra K. Pandit
- Book ID
- 104589152
- Publisher
- Elsevier Science
- Year
- 2010
- Tongue
- English
- Weight
- 159 KB
- Volume
- 109
- Category
- Article
- ISSN
- 0165-0513
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✦ Synopsis
Abstract
1‐(5‐uracilylmethyl)pyridinium salts react with 9, 10‐dihydrophenanthridine, Hantzsch ester or thiols (RSH, R = p‐nitrobenzyl, t‐butyl) to form thymine derivatives. The mechanisms of the reactions are discussed.
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