التفاصيل البيبلوغرافية
العنوان: |
A portal to highly valuable indole-functionalized vinyl sulfonyl fluorides and allylic sulfonyl fluorides. |
المؤلفون: |
Huang W; State Key Laboratory of Silicate Materials for Architectures; and School of Chemistry, Chemical Engineering and Life Sciences, Wuhan University of Technology, Wuhan 430070, China. qinhuali@whut.edu.cn., Fayad E; Department of Biotechnology, College of Sciences, Taif University, P.O. Box 11099, Taif 21944, Saudi Arabia. e.esmail@tu.edu.sa., Abu Ali OA; Department of Chemistry, College of Science, Taif University, Taif 21944, Saudi Arabia. o.abuali@tu.edu.sa., Qin HL; State Key Laboratory of Silicate Materials for Architectures; and School of Chemistry, Chemical Engineering and Life Sciences, Wuhan University of Technology, Wuhan 430070, China. qinhuali@whut.edu.cn. |
المصدر: |
Organic & biomolecular chemistry [Org Biomol Chem] 2024 Sep 11; Vol. 22 (35), pp. 7117-7120. Date of Electronic Publication: 2024 Sep 11. |
نوع المنشور: |
Journal Article |
اللغة: |
English |
بيانات الدورية: |
Publisher: Royal Society of Chemistry Country of Publication: England NLM ID: 101154995 Publication Model: Electronic Cited Medium: Internet ISSN: 1477-0539 (Electronic) Linking ISSN: 14770520 NLM ISO Abbreviation: Org Biomol Chem Subsets: PubMed not MEDLINE; MEDLINE |
أسماء مطبوعة: |
Original Publication: Cambridge, UK : Royal Society of Chemistry, c2003- |
مستخلص: |
A practical and efficient method for the C-3 site selective alkenylation of indoles was developed for constructing novel indole-functionalized vinyl sulfonyl fluorides and indolyl allylic sulfonyl fluorides. The reaction is accomplished with exclusive regio- and stereoselectivity without using transition metal catalysts, providing novel products of great potential value in medicinal chemistry, chemical biology, and drug discovery. |
تواريخ الأحداث: |
Date Created: 20240816 Latest Revision: 20240911 |
رمز التحديث: |
20240911 |
DOI: |
10.1039/d4ob01213e |
PMID: |
39150283 |
قاعدة البيانات: |
MEDLINE |