http://rdf.ncbi.nlm.nih.gov/pubchem/reference/22254727

Outgoing Links

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contentType Journal Article|Research Support, Non-U.S. Gov't
endingPage 6284
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issueIdentifier 21
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publicationName Angewandte Chemie (International ed. in English)
startingPage 6280
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bibliographicCitation Yang L, Lin Z, Huang SH, Hong R. Stereodivergent Synthesis of Functionalized Tetrahydropyrans Accelerated by Mechanism-Based Allylboration and Bioinspired Oxa-Michael Cyclization. Angew Chem Int Ed Engl. 2016 May 17;55(21):6280–4. doi: 10.1002/anie.201600558. PMID: 27072483.
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date 2016-04-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier https://doi.org/10.1002/anie.201600558
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language English
source https://pubmed.ncbi.nlm.nih.gov/
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title Stereodivergent Synthesis of Functionalized Tetrahydropyrans Accelerated by Mechanism‐Based Allylboration and Bioinspired Oxa‐Michael Cyclization
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Total number of triples: 30.