The 5′,6-Oxomethylene Transglycosidic Tether for Conformational Restriction of Pyrimidine Ribonucleosides. Investigation of 6-Formyl- and 6-(Hydroxymethyl)uridine 5′-Carboxaldehydes-Reference-Cited by-同舟云学术

The 5′,6-Oxomethylene Transglycosidic Tether for Conformational Restriction of Pyrimidine Ribonucleosides. Investigation of 6-Formyl- and 6-(Hydroxymethyl)uridine 5′-Carboxaldehydes

Published:2000-12 Issue:51 Volume:56 Page:9885-9893
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Groziak Michael P.,Lin Ronghui

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference44 articles.

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3. (j) Tusa, G.; Reed, J. K. Nucleosides Nucleotides Nucleic Acids 2000, 19, 805–813. An intramolecularly cyclized 5′-uridylic acid featuring a tether between the pyrimidine C5 and the phosphate group is exceedingly biomimetic, lacking only one of the ionizing P–OH groups:

4. (k) Seio, K.; Wada, T.; Sakamoto, K.; Yokoyama, S.; Sekine, M. J. Org. Chem. 1996, 61, 1500–1504.

5. (l) Sekine, M.; Kurasawa, O.; Shohda, K.-i.; Seio, K.; Wada, T. J. Org. Chem. 2000, 65, 3571–3578.

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