Facile syntheses of pseudo-α-d-arabinofuranose, and two pseudo-d-arabinofuranosylnucleosides, (+)-cyclaradine and (+)-1-pseudo-β-d-arabinofuranosyluracil, from d-arabinose-Reference-Cited by-同舟云学术

Facile syntheses of pseudo-α-d-arabinofuranose, and two pseudo-d-arabinofuranosylnucleosides, (+)-cyclaradine and (+)-1-pseudo-β-d-arabinofuranosyluracil, from d-arabinose

Published:1994-01 Issue:33 Volume:50 Page:9961-9974
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Yoshikawa Masayuki,Yokokawa Yoshihiro,Inoue Yasunao,Yamaguchi Shoko,Murakami Nobutoshi,Kitagawa Isao

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference27 articles.

1. This work was partly reported in our preliminary communication, M. Yoshikawa ,N. Murakami, Y. Inoue, S. Hatakeyama, and I. Kitagawa, Chem. Pharm. Bull., 41, 636-638.

2. Alicyclic Carbohydrates. XXIX.1,2 The Synthesis of a Pseudo-Hexose (2,3,4,5-Tetrahydroxycyclohexanemethanol)

3. 9-[β-DL-2α,3α-Dihydroxy-4β-(hydroxymethyl)- cyclopentyl]adenine, the Carbocyclic Analog of Adenosine1,2

4. Synthesis of carbocyclic analogs of purine ribonucleosides

5. Isolation of a cyclitol antibiotic: 2,3,4,5-tetrahydroxycyclohexanemethanol

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