| Gold catalyzed stereoselective tandem hydroamination-formal aza-Diels-Alder reaction of propargylic amino esters. | |
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MedLine Citation:
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PMID: 23303342 Owner: NLM Status: Publisher |
Abstract/OtherAbstract:
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A gold-catalyzed tandem intramolecular hydroamination-formal aza-Diels-Alder reaction of propargylic amino esters is described. The overall process leads to the formation of a tetracyclic framework as a single diastereoisomer, with the creation of four bonds and five stereocenters. |
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Authors:
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Santos Fustero; Paula Bello; Javier Miró; María Sánchez-Roselló; Miguel A Maestro; Javier González; Carlos Del Pozo |
Publication Detail:
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Type: JOURNAL ARTICLE Date: 2013-1-10 |
Journal Detail:
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Title: Chemical communications (Cambridge, England) Volume: - ISSN: 1364-548X ISO Abbreviation: Chem. Commun. (Camb.) Publication Date: 2013 Jan |
Date Detail:
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Created Date: 2013-1-10 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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Dept. de Química Orgánica, Universidad de Valencia, E-46100, Burjassot, Spain. santos.fustero@uv.es carlos.pozo@uv.es. |
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From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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