Facile synthesis of the spiro-pyridoindolone scaffold via a gold-catalysed intramolecular alkynol cyclisation/hydroindolylation
Title | Facile synthesis of the spiro-pyridoindolone scaffold via a gold-catalysed intramolecular alkynol cyclisation/hydroindolylation |
Publication Type | Journal Article |
Year of Publication | 2022 |
Authors | Shinde, MH, V. Ramana, C |
Journal | Organic & Biomolecular Chemistry |
Volume | 20 |
Issue | 10 |
Pagination | d1ob02483c |
Date Published | MAR |
Type of Article | Article |
ISSN | 1477-0520 |
Abstract | A simple approach for the synthesis of pyridoindolone scaffolds with a spiroannulated tetrahydrofuran ring is described. The overall process comprises intramolecular sequential gold-catalysed 5-endo-dig alkynol cycloisomerization and subsequent addition of indole C2 to the in situ generated oxocarbenium cation. |
DOI | 10.1039/d1ob02483c |
Type of Journal (Indian or Foreign) | Foreign |
Impact Factor (IF) | 3.890 |
Divison category:
Organic Chemistry
Database:
Web of Science (WoS)
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