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Object |
contentType |
Journal Article|Research Support, Non-U.S. Gov't|Research Support, U.S. Gov't, Non-P.H.S.|Research Support, U.S. Gov't, P.H.S. |
endingPage |
12603 |
issn |
1520-5126 0002-7863 |
issueIdentifier |
39 |
pageRange |
12596-12603 |
publicationName |
Journal of the American Chemical Society |
startingPage |
12596 |
hasFundingAgency |
http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_a1ebfe17b0713ecaf89801f0370c078d |
isSupportedBy |
http://rdf.ncbi.nlm.nih.gov/pubchem/grant/MD5_341d01573e2d520f95c64d04dbfa35a4 |
bibliographicCitation |
Wang L, Seiders JR, Floreancig PE. Structure-reactivity relationships in oxidative carbon-carbon bond forming reactions: a mild and efficient approach to stereoselective syntheses of 2,6-disubstituted tetrahydropyrones. J Am Chem Soc. 2004 Oct 06;126(39):12596–603. doi: 10.1021/ja046125b. PMID: 15453792. |
creator |
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_4e522ae25804f024a2b9df0c2e6fe1aa http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_af006cfa6f57eaaf60f82ac3b55a3949 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_27f8de5100a784f8a427f178a09b7ec8 |
date |
2004-09-11-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
identifier |
https://pubmed.ncbi.nlm.nih.gov/15453792 https://doi.org/10.1021/ja046125b |
isPartOf |
https://portal.issn.org/resource/ISSN/1520-5126 https://portal.issn.org/resource/ISSN/0002-7863 http://rdf.ncbi.nlm.nih.gov/pubchem/journal/4435 |
language |
English |
source |
https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/ |
title |
Structure−Reactivity Relationships in Oxidative Carbon−Carbon Bond Forming Reactions: A Mild and Efficient Approach to Stereoselective Syntheses of 2,6-Disubstituted Tetrahydropyrones |
discusses |
http://id.nlm.nih.gov/mesh/M0018272 http://id.nlm.nih.gov/mesh/M0008827 |
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http://id.nlm.nih.gov/mesh/D011753Q000138 |
hasSubjectTerm |
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discussesAsDerivedByTextMining |
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID5462310 http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7765 |