Transition-Metal-Free, Bronsted Acid-Mediated Cascade Sequence in the Reaction of Propargyl Alcohols with Sulfonamido-indoles/- indolines: Highly Substituted delta- and alpha-Carbolines
Bronsted acid-mediated, transition-metal-free reaction of propargyl alcohols with sulfonamido-indoles/indolines under mild conditions affords highly substituted delta- or alpha-carbolines in good to excellent yields. This protocol involves cascade reaction sequences of Friedel Crafts alkylation/ [1,...
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| Published in: | Journal of organic chemistry Vol. 83; no. 24; pp. 15043 - 15056 |
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| Main Authors: | , |
| Format: | Journal Article |
| Language: | English |
| Published: |
WASHINGTON
Amer Chemical Soc
21.12.2018
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| Subjects: | |
| ISSN: | 0022-3263, 1520-6904, 1520-6904 |
| Online Access: | Get more information |
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| Summary: | Bronsted acid-mediated, transition-metal-free reaction of propargyl alcohols with sulfonamido-indoles/indolines under mild conditions affords highly substituted delta- or alpha-carbolines in good to excellent yields. This protocol involves cascade reaction sequences of Friedel Crafts alkylation/ [1,5]-hydrogen shift/electrocyclization/elimination/ [1,2]-aryl migration followed by aromatization. An unexpected regioselective tosyl group migration from indole 2- to 6-position and arene elimination leading to alpha-carbolines has also been discovered. |
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| Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
| ISSN: | 0022-3263 1520-6904 1520-6904 |
| DOI: | 10.1021/acs.joc.8b02293 |