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Object |
contentType |
Journal Article|Research Support, Non-U.S. Gov't |
endingPage |
6284 |
issn |
1433-7851 1521-3773 |
issueIdentifier |
21 |
pageRange |
6280-6284 |
publicationName |
Angewandte Chemie (International ed. in English) |
startingPage |
6280 |
hasFundingAgency |
http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_3f17f4f22da1fec23e4714e45f8dd7f2 http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_462d2b4cdaaff677d13b8a6bafd8b900 http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_487baf6554eb36bb22c6138d90a7c50f |
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. |
creator |
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_d9ce6ca5ffd29b7e3d175d91b1842646 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_a4d98a9eb61ec94bb044aeb8ace2a695 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_f749cfdca0d90dd1b6d4e4932dc98ecc http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_3dbe9aaebf9178e54943ee7511aea997 |
date |
2016-04-13-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
identifier |
https://doi.org/10.1002/anie.201600558 https://pubmed.ncbi.nlm.nih.gov/27072483 |
isPartOf |
http://rdf.ncbi.nlm.nih.gov/pubchem/journal/537 https://portal.issn.org/resource/ISSN/1521-3773 https://portal.issn.org/resource/ISSN/1433-7851 |
language |
English |
source |
https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/ |
title |
Stereodivergent Synthesis of Functionalized Tetrahydropyrans Accelerated by Mechanism‐Based Allylboration and Bioinspired Oxa‐Michael Cyclization |
discussesAsDerivedByTextMining |
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID11150526 http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID24899382 http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID10037 http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID177 |