reference/22044716

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/22044716

Outgoing Links

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contentType	Journal Article\|Research Support, N.I.H., Extramural\|Research Support, U.S. Gov't, Non-P.H.S.\|Research Support, U.S. Gov't, P.H.S.
endingPage	2119
issn	1520-6904 0022-3263
issueIdentifier	6
pageRange	2109-2119
publicationName	The Journal of Organic Chemistry
startingPage	2109
hasFundingAgency	http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_a1ebfe17b0713ecaf89801f0370c078d
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bibliographicCitation	Dieter RK, Chen N, Yu H, Nice LE, Gore VK. Reaction of alpha-(N-carbamoyl)alkylcuprates with propargyl substrates: synthetic route to alpha-amino allenes and delta3-pyrrolines. J Org Chem. 2005 Mar 18;70(6):2109–19. doi: 10.1021/jo0481405. PMID: 15760194.
creator	http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_8531a4cdc4af6e4c82c20f74aea2f6d2 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_a5e792d6fcec096647f52dd5d9bdb152 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_876d967c8e8d7bddd0d394fbec42694c http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_083bf9d3f27bcceb52079f7f1956a436 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_75b7c3fb072e7365a6dc91efd2f480e5
date	2005-02-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://doi.org/10.1021/jo0481405 https://pubmed.ncbi.nlm.nih.gov/15760194
isPartOf	http://rdf.ncbi.nlm.nih.gov/pubchem/journal/5098 https://portal.issn.org/resource/ISSN/0022-3263 https://portal.issn.org/resource/ISSN/1520-6904
language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	Reaction of α-(N-Carbamoyl)alkylcuprates with Propargyl Substrates: Synthetic Route to α-Amino Allenes and Δ3-Pyrrolines
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Incoming Links

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Total number of triples: 48.