17O NMR of diastereomeric 3′,5′-cyclic thymidine methyl phosphates, methylphosphonates, and N,N-dimethyl phosphoramidates. Phosphorus configuration of P-chiral [17O, 18O]-nucleoside phosphate diesters-Reference-Cited by-同舟云学术

17O NMR of diastereomeric 3′,5′-cyclic thymidine methyl phosphates, methylphosphonates, and N,N-dimethyl phosphoramidates. Phosphorus configuration of P-chiral [17O, 18O]-nucleoside phosphate diesters

Published:1989-01 Issue:10 Volume:30 Page:1221-1224
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Sopchik Alan E.,Cairns S. Matthew,Bentrude Wesley G.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference18 articles.

1. Oxygen-17 NMR spectral properties of simple phosphate esters and adenine nucleotides

2. Does the magnesium(II) ion interact with the .alpha.-phosphate of ATP? An investigation by oxygen-17 nuclear magnetic resonance

3. Oxygen chiral phosphodiesters. 3. Use of oxygen-17 NMR spectroscopy to demonstrate configurational differences in the diastereomers of cyclic 2'-deoxyadenosine 3',5'-[17O,18O]monophosphate

4. Syntheses and configurational analyses of thymidine 4-nitrophenyl [17O,18O]phosphates and the stereochemical course of a reaction catalyzed by bovine pancreatic deoxyribonuclease I

5. Oxygen-17 NMR spectral properties of simple phosphate esters and adenine nucleotides

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