Predicate |
Object |
contentType |
Journal Article |
endingPage |
2992 |
issn |
1523-7052 1523-7060 |
issueIdentifier |
17 |
pageRange |
2989-2992 |
publicationName |
Organic Letters |
startingPage |
2989 |
bibliographicCitation |
Ma S, Gao W. Tuning the reaction paths in palladium(0)-catalyzed coupling-cyclization reaction of beta-amino allenes with organic halides: a substituent switch. Org Lett. 2002 Aug 22;4(17):2989–92. doi: 10.1021/ol026406t. PMID: 12182606. |
creator |
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_3398be359a0a24c3e6494744274e2926 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_54586cd467d5b80bfc8d85a0285def6e |
date |
2002-07-18-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
identifier |
https://pubmed.ncbi.nlm.nih.gov/12182606 https://doi.org/10.1021/ol026406t |
isPartOf |
https://portal.issn.org/resource/ISSN/1523-7060 http://rdf.ncbi.nlm.nih.gov/pubchem/journal/21677 https://portal.issn.org/resource/ISSN/1523-7052 |
language |
English |
source |
https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/ |
title |
Tuning the reaction paths in palladium(0)-catalyzed coupling-cyclization reaction of beta-amino allenes with organic halides: a substituent switch |
discussesAsDerivedByTextMining |
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID10037 http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID23938 |