A General Synthesis of Pyrimidine Nucleosides
1970; Wiley; Volume: 9; Issue: 6 Linguagem: Inglês
10.1002/anie.197004612
ISSN1521-3773
AutoresUlrich Niedballa, Helmut Vorbrüggen,
Tópico(s)HIV/AIDS drug development and treatment
ResumoAngewandte Chemie International Edition in EnglishVolume 9, Issue 6 p. 461-462 Communication A General Synthesis of Pyrimidine Nucleosides† Dr. U. Niedballa, Dr. U. Niedballa Experimentelle Forschung Pharma der Schering AG, 1 Berlin 65, Müllerstrasse 170–172 (Germany)Search for more papers by this authorDr. Helmut Vorbrüggen, Corresponding Author Dr. Helmut Vorbrüggen Experimentelle Forschung Pharma der Schering AG, 1 Berlin 65, Müllerstrasse 170–172 (Germany)Experimentelle Forschung Pharma der Schering AG, 1 Berlin 65, Müllerstrasse 170–172 (Germany)Search for more papers by this author Dr. U. Niedballa, Dr. U. Niedballa Experimentelle Forschung Pharma der Schering AG, 1 Berlin 65, Müllerstrasse 170–172 (Germany)Search for more papers by this authorDr. Helmut Vorbrüggen, Corresponding Author Dr. Helmut Vorbrüggen Experimentelle Forschung Pharma der Schering AG, 1 Berlin 65, Müllerstrasse 170–172 (Germany)Experimentelle Forschung Pharma der Schering AG, 1 Berlin 65, Müllerstrasse 170–172 (Germany)Search for more papers by this author First published: June 1970 https://doi.org/10.1002/anie.197004612Citations: 145 † Synthesis of Nucleosides, Part 3. – Part 2: H. Vorbrüggen and P. Strehlke, Angew. Chem. 81, 998 (1969); Angew. Chem. internat. Edit. 8, 977 (1969). AboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onEmailFacebookTwitterLinkedInRedditWechat No abstract is available for this article. References 1 J. J. Fox, N. Yung, J. Davoll, and G. B. Brown, J. Amer. chem. Soc. 78, 2117 (1956); 10.1021/ja01591a024 CASWeb of Science®Google Scholar K. A. Watanabe and J. J. Fox, J. heterocyclic Chem. 6, 109 (1969); 10.1002/jhet.5570060119 CASWeb of Science®Google Scholar I. A. Mikhailopulo, V. I. Gunar, and S. I. Zav'yabov, Izvest. Akad. Nauk SSSR, Ser. chim. 1967, 470; Google Scholar G. T. Rogers, R. S. Shadbolt, and T. L. V. Ulbricht, J. chem. Soc. (London) C 1969, 203. Google Scholar 1a J. Pliml and M. Prystas, Advances in Heterocyclic Chemistry 8, 115. 10.1016/S0065-2725(08)60605-4 CASGoogle Scholar 2 T. Nishimura, B. Shimizu, and I. Iwai, Chem. pharmac. Bull. (Japan) 11, 1470 (1963); 10.1248/cpb.11.1470 CASPubMedGoogle Scholar E. Wittenburg, Z. Chem. 4, 303 (1964). 10.1002/zfch.19640040806 CASGoogle Scholar 3 H. Vorbrüggen and P. Strehlke, Angew. Chem. 81, 997 (1969); 10.1002/ange.19690812308 Google Scholar Angew. Chem. internat. Edit. 8, 976 (1969). CASGoogle Scholar 4 E. Wittenburg, Chem. Ber. 101, 1095 (1968). 10.1002/cber.19681010346 CASPubMedWeb of Science®Google Scholar Citing Literature Volume9, Issue6June 1970Pages 461-462 ReferencesRelatedInformation
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