A novel stereospecific radical cyclization of 2′,3′-O-isopropylideneuridine and -adenosine 5′-aldehyde to the corresponding 6,5′-cyclodihydrouridine and 8,5′-cycloadenosine derivatives-Reference-Cited by-同舟云学术

A novel stereospecific radical cyclization of 2′,3′-O-isopropylideneuridine and -adenosine 5′-aldehyde to the corresponding 6,5′-cyclodihydrouridine and 8,5′-cycloadenosine derivatives

Published:1988-01 Issue:1 Volume:29 Page:75-78
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Sugawara Tomokazu,Otter Brian A.,Ueda Tohru

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference15 articles.

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2. Reductive cyclizations involving attack of radical anions derived from ketones, aldehydes and enones on isolated carbon-carbon triple and double bonds. Application of frontier molecular orbitals

3. Conversion of ketones having δ, ϵ-π-functions to cyclopentanols by zinc-trimethylchlorosilane

4. Reductive, radical-induced cyclization of 5-hexenals as a biomimetic model of the chemistry of secologanin formation

5. Synthesis and molecular conformation of 2′,3′-O-isopropylidene-5′-deoxy-6(R),5′-cyclo-5,6-dihydrouridine

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