Nucleosides and Nucleotides. 151. Conversion of (Z)-2‘-(Cyanomethylene)-2‘-deoxyuridines into Their (E)-Isomers via Addition of Thiophenol to the Cyanomethylene Moiety Followed by Oxidative Syn-elimination Reactions1-Reference-Cited by-同舟云学术

Nucleosides and Nucleotides. 151. Conversion of (Z)-2‘-(Cyanomethylene)-2‘-deoxyuridines into Their (E)-Isomers via Addition of Thiophenol to the Cyanomethylene Moiety Followed by Oxidative Syn-elimination Reactions1

Published:1996-01-01 Issue:18 Volume:61 Page:6261-6267
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Hassan Abdalla E. A.¹,Nishizono Naozumi¹,Minakawa Noriaki¹,Shuto Satoshi¹,Matsuda Akira¹

Affiliation:

1. Faculty of Pharmaceutical Sciences, Hokkaido University, Kita-12, Nishi-6, Kita-ku, Sapporo 060, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo960577s

Reference34 articles.

1. Nucleosides and nucleotides. 83. Design, synthesis, and antineoplastic activity of 2'-deoxy-2'-methylidenecytidine

2. Nucleosides and nucleotides. 97. Synthesis of new broad spectrum antineoplastic nucleosides, 2'-deoxy-2'-methylidenecytidine (DMDC) and its derivatives

3. (d) Matsuda, A.; Azuma, A.; Nakajima, Y.; Takenuki, K.; Dan, A.; Iino, T.; Yoshimura, Y.; Minakawa, N.; Tanaka, M.; Sasaki, T. InNucleosides and Nucleotides as Antitumor and Antiviral Agents; Chu, C. K., Baker, D. C., Eds.; Plenum Publishing Co. New York, 1993; pp 1−22.

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