دورية أكاديمية

Transition-metal-free catalytic synthesis of 1,5-diaryl-1,2,3-triazoles.

التفاصيل البيبلوغرافية
العنوان: Transition-metal-free catalytic synthesis of 1,5-diaryl-1,2,3-triazoles.
المؤلفون: Kwok SW; The Scripps Research Institute, La Jolla, California 92037, USA., Fotsing JR, Fraser RJ, Rodionov VO, Fokin VV
المصدر: Organic letters [Org Lett] 2010 Oct 01; Vol. 12 (19), pp. 4217-9.
نوع المنشور: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
اللغة: English
بيانات الدورية: Publisher: American Chemical Society Country of Publication: United States NLM ID: 100890393 Publication Model: Print Cited Medium: Internet ISSN: 1523-7052 (Electronic) Linking ISSN: 15237052 NLM ISO Abbreviation: Org Lett Subsets: MEDLINE
أسماء مطبوعة: Original Publication: Washington, DC : American Chemical Society, c1999-
مواضيع طبية MeSH: Triazoles/*chemical synthesis, Catalysis ; Hydroxides/chemistry ; Molecular Structure ; Transition Elements/chemistry
مستخلص: 1,5-Diarylsubstituted 1,2,3-triazoles are formed in high yield from aryl azides and terminal alkynes in DMSO in the presence of catalytic tetraalkylammonium hydroxide. The reaction is experimentally simple, does not require a transition-metal catalyst, and is not sensitive to atmospheric oxygen and moisture.
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معلومات مُعتمدة: R01 GM087620 United States GM NIGMS NIH HHS; GM087620 United States GM NIGMS NIH HHS
المشرفين على المادة: 0 (Hydroxides)
0 (Transition Elements)
0 (Triazoles)
تواريخ الأحداث: Date Created: 20100910 Date Completed: 20110106 Latest Revision: 20211020
رمز التحديث: 20240628
مُعرف محوري في PubMed: PMC2946857
DOI: 10.1021/ol101568d
PMID: 20825167
قاعدة البيانات: MEDLINE
الوصف
تدمد:1523-7052
DOI:10.1021/ol101568d