| Kinetic resolution of racemic 2,3-allenoates by organocatalytic asymmetric 1,3-dipolar cycloaddition. | |
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MedLine Citation:
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PMID: 20715835 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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The kinetic resolution of racemic 2,3-allenoates was realized via 1,3-dipolar cycloaddition by using a bisphosphoric acid catalyst, affording the optically active 2,3-allenoates and 3-methylenepyrrolidine derivatives in high yields and enantioselectivities. |
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Authors:
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Jie Yu; Wei-Jie Chen; Liu-Zhu Gong |
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Publication Detail:
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Type: Journal Article; Research Support, Non-U.S. Gov't |
Journal Detail:
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Title: Organic letters Volume: 12 ISSN: 1523-7052 ISO Abbreviation: Org. Lett. Publication Date: 2010 Sep |
Date Detail:
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Created Date: 2010-09-10 Completed Date: 2010-12-21 Revised Date: - |
Medline Journal Info:
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Nlm Unique ID: 100890393 Medline TA: Org Lett Country: United States |
Other Details:
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Languages: eng Pagination: 4050-3 Citation Subset: IM |
Affiliation:
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Hefei National Laboratory for Physical Sciences at the Microscale and Department of Chemistry, University of Science and Technology of China, Hefei 230026, China. |
Export Citation:
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| MeSH Terms | |
Descriptor/Qualifier:
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Catalysis Cyclization Kinetics Models, Molecular Molecular Structure Naphthalenes / chemistry* Stereoisomerism |
| Chemical | |
Reg. No./Substance:
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0/Naphthalenes; 553-39-9/allenolic acid |
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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