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One-Pot Conversion of Serine and α-Methylserine Derivatives to the Corresponding Cysteines and Selenocystines by Using Chalcogenophosphate Reagents.
- Source :
- Phosphorus, Sulfur & Silicon & the Related Elements; Jan2011, Vol. 186 Issue 1, p125-133, 9p, 4 Diagrams, 2 Charts
- Publication Year :
- 2011
-
Abstract
- The one-pot reactions of N-acetylserine methyl ester and N-acetyl-α-methylserine methyl ester with Lawesson's or Woollins' reagent directly produced the corresponding cysteine or selenocysteine derivatives in moderate yields. The transformation would be initiated by phosphorylation of the hydroxy group, rather than chalcogenation of the amide group, and involve the oxazoline as a key intermediate. Supplemental materials are available for this article. Go to the publisher's online edition of Phosphorus, Sulfur, and Silicon and the Related Elements to view the free supplemental file. GRAPHICAL ABSTRACT[image omitted] [ABSTRACT FROM AUTHOR]
- Subjects :
- SERINE
CHEMICAL reagents
SULFUR
SELENIUM
AMINO acids
ALCOHOLS (Chemical class)
THIOLS
Subjects
Details
- Language :
- English
- ISSN :
- 10426507
- Volume :
- 186
- Issue :
- 1
- Database :
- Complementary Index
- Journal :
- Phosphorus, Sulfur & Silicon & the Related Elements
- Publication Type :
- Academic Journal
- Accession number :
- 57378362
- Full Text :
- https://doi.org/10.1080/10426507.2010.485155