Synthesis of the four possible stereoisomeric 5′-nor carbocyclic nucleosides from one common enantiomerically pure starting material-Reference-Cited by-同舟云学术

Synthesis of the four possible stereoisomeric 5′-nor carbocyclic nucleosides from one common enantiomerically pure starting material

Published:1994-03 Issue:13 Volume:35 Page:1961-1964
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Dyatkina Natalja,Costisella Burkhard,Theil Fritz,von Janta-Lipinski Martin

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference13 articles.

1. The synthesis and antiviral properties of (.+-.)-5'-noraristeromycin and related purine carbocyclic nucleosides. A new lead for anti-human cytomegalovirus agent design

2. Synthesis of chiral carbocyclic nucleosides

3. Maxeiner, H.G.; Dyatkina, N.; Matthes, E.; von Janta-Lipinski, M.; Habermehl, K.O.; Langen, P. VIIIth International Congress of Virology, Abstract of Papers, page 328, Berlin, 26.-31.8.1990

4. Lipase-catalyzed transesterification of meso-cyclopentane diols

5. Enzymatic hydrolysis of prochiral -1,4-diacyl-2-cyc-lopentenediols: preparation of (1,4)-and (1,4)-4-hydroxy-2-cyclopentenylderivatives, versatile building blocks for cyclopentanoid natural products.

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