Nucleosidtransformationen, 2: Selektive Oxiranringöffnung von 9‐(2,3‐Anhydro‐β‐ D ‐ribofuranosyl)‐ und 9‐(2,3‐Anhydro‐β‐ D ‐lyxofuranosyl)adenin-Reference-Cited by-同舟云学术

Nucleosidtransformationen, 2: Selektive Oxiranringöffnung von 9‐(2,3‐Anhydro‐β‐ D ‐ribofuranosyl)‐ und 9‐(2,3‐Anhydro‐β‐ D ‐lyxofuranosyl)adenin

Published:1976-04 Issue:4 Volume:109 Page:1395-1406
ISSN:0009-2940
Container-title:Chemische Berichte
language:en
Short-container-title:Chem. Ber.

Author:

Mengel Rudolf¹,Wiedner Harald¹

Affiliation:

1. Fachbereich Chemie der Universität Konstanz, D‐7750 Konstanz, Postfach 7333

Publisher

Wiley

Subject

Inorganic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/cber.19761090422

Reference27 articles.

1. (1a) 1. Mitteil. s. 1. c.10.‐ 1b) Teilweise vorgetragen am 29. Oktober1974auf der Tagung „Nucleosides et activities biologiques”︁ in Montpellier Frankreich.

2. CHEMICAL SYNTHESES AND TRANSFORMATIONS OF NUCLEOSIDES

3. Nucleic acid related compounds. II. Adenosine 2',3'-ribo-epoxide. Synthesis, intramolecular degradation, and transformation into 3'-substituted xylofuranosyl nucleosides and the lyxo-epoxide

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