| Lewis acid-catalyzed Friedel-Crafts alkylations of 3-hydroxy-2-oxindole: an efficient approach to the core structure of azonazine. | |
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MedLine Citation:
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PMID: 22962662 Owner: NLM Status: Publisher |
Abstract/OtherAbstract:
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A Lewis acid catalyzed Friedel-Crafts reaction of electron rich aromatics with 3-alkyl-3-hydroxy-2-oxindole () has been developed. The methodology provides a straightforward access to the core of azonazine () sharing an all-carbon quaternary stereocenter at the tetracyclic ring junction. |
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Authors:
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Santanu Ghosh; Lakshmana K Kinthada; Subhajit Bhunia; Alakesh Bisai |
Publication Detail:
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Type: JOURNAL ARTICLE Date: 2012-9-7 |
Journal Detail:
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Title: Chemical communications (Cambridge, England) Volume: - ISSN: 1364-548X ISO Abbreviation: Chem. Commun. (Camb.) Publication Date: 2012 Sep |
Date Detail:
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Created Date: 2012-9-10 Completed Date: - Revised Date: - |
Medline Journal Info:
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Nlm Unique ID: 9610838 Medline TA: Chem Commun (Camb) Country: - |
Other Details:
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Languages: ENG Pagination: - Citation Subset: - |
Affiliation:
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Department of Chemistry, Indian Institute of Science Education and Research Bhopal, Bhopal, MP 460 023, India. alakesh@iiserb.ac.in. |
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From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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