http://rdf.ncbi.nlm.nih.gov/pubchem/reference/12520919

Outgoing Links

Predicate Object
contentType Journal Article
endingPage 5867
issn 1520-6904
0022-3263
issueIdentifier 16
pageRange 5864-5867
publicationName The Journal of Organic Chemistry
startingPage 5864
bibliographicCitation Inoue H, Nagaoka Y, Tomioka K. A new methodology for synthesis of a chiral phosphinocarboxylic acid through Michael cyclization-aldol tandem reaction of chiral alpha,beta,chi,psi-unsaturated bisphosphine oxide and application in palladium-catalyzed asymmetric allylic alkylation. J Org Chem. 2002 Aug 09;67(16):5864–7. doi: 10.1021/jo025725v. PMID: 12153296.
creator http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_3cbaa4db6af619672cf544a53d169135
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_a6888869dfebc2bc785e5476caee2986
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_cbb38b17202ee161e9801228de3b2c07
date 2002-07-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier https://pubmed.ncbi.nlm.nih.gov/12153296
https://doi.org/10.1021/jo025725v
isPartOf https://portal.issn.org/resource/ISSN/1520-6904
https://portal.issn.org/resource/ISSN/0022-3263
http://rdf.ncbi.nlm.nih.gov/pubchem/journal/5098
language English
source https://www.crossref.org/
https://pubmed.ncbi.nlm.nih.gov/
title A new methodology for synthesis of a chiral phosphinocarboxylic acid through Michael cyclization-aldol tandem reaction of chiral alpha,beta,chi,psi-unsaturated bisphosphine oxide and application in palladium-catalyzed asymmetric allylic alkylation
discussesAsDerivedByTextMining http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID190217
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID240
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID2724682
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID23938
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID14345805

Incoming Links

Predicate Subject
isDiscussedBy http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID129340886
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID128115233
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID128585334

Total number of triples: 30.