http://rdf.ncbi.nlm.nih.gov/pubchem/reference/11828915

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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
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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
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Predicate Subject
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Total number of triples: 24.