| pubmed-article:8180658 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:8180658 | lifeskim:mentions | umls-concept:C0002520 | lld:lifeskim |
| pubmed-article:8180658 | lifeskim:mentions | umls-concept:C0017110 | lld:lifeskim |
| pubmed-article:8180658 | lifeskim:mentions | umls-concept:C0443286 | lld:lifeskim |
| pubmed-article:8180658 | lifeskim:mentions | umls-concept:C1511790 | lld:lifeskim |
| pubmed-article:8180658 | lifeskim:mentions | umls-concept:C0596801 | lld:lifeskim |
| pubmed-article:8180658 | lifeskim:mentions | umls-concept:C0024868 | lld:lifeskim |
| pubmed-article:8180658 | lifeskim:mentions | umls-concept:C0936012 | lld:lifeskim |
| pubmed-article:8180658 | lifeskim:mentions | umls-concept:C0521115 | lld:lifeskim |
| pubmed-article:8180658 | lifeskim:mentions | umls-concept:C0598132 | lld:lifeskim |
| pubmed-article:8180658 | pubmed:issue | 1 | lld:pubmed |
| pubmed-article:8180658 | pubmed:dateCreated | 1994-6-14 | lld:pubmed |
| pubmed-article:8180658 | pubmed:abstractText | The one-step ethyl chloroformate derivatization of amino acids in an aqueous medium is extended with the use of a variety of alkyl chloroformate reagents. This provides a new and convenient procedure for preparing esters with different alkoxy groups. A new mechanism for esterification during chloroformate derivatization is proposed based on the formation of an intermediate mixed carboxylic-carbonic acid anhydride followed by the exchange with an alcohol. Among the different reagents investigated, isobutyl chloroformate derivatized amino acids were found to provide more sensitivity for analyses by GC-flame ionization detection and GC-MS relative to derivatives prepared by other alkyl chloroformates. | lld:pubmed |
| pubmed-article:8180658 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:8180658 | pubmed:language | eng | lld:pubmed |
| pubmed-article:8180658 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:8180658 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:8180658 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:8180658 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:8180658 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:8180658 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:8180658 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:8180658 | pubmed:month | Mar | lld:pubmed |
| pubmed-article:8180658 | pubmed:issn | 0021-9673 | lld:pubmed |
| pubmed-article:8180658 | pubmed:author | pubmed-author:WangJJ | lld:pubmed |
| pubmed-article:8180658 | pubmed:author | pubmed-author:WatsonJ TJT | lld:pubmed |
| pubmed-article:8180658 | pubmed:author | pubmed-author:HuangZ HZH | lld:pubmed |
| pubmed-article:8180658 | pubmed:author | pubmed-author:GageD ADA | lld:pubmed |
| pubmed-article:8180658 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:8180658 | pubmed:day | 4 | lld:pubmed |
| pubmed-article:8180658 | pubmed:volume | 663 | lld:pubmed |
| pubmed-article:8180658 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:8180658 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:8180658 | pubmed:pagination | 71-8 | lld:pubmed |
| pubmed-article:8180658 | pubmed:dateRevised | 2009-1-15 | lld:pubmed |
| pubmed-article:8180658 | pubmed:meshHeading | pubmed-meshheading:8180658-... | lld:pubmed |
| pubmed-article:8180658 | pubmed:meshHeading | pubmed-meshheading:8180658-... | lld:pubmed |
| pubmed-article:8180658 | pubmed:meshHeading | pubmed-meshheading:8180658-... | lld:pubmed |
| pubmed-article:8180658 | pubmed:meshHeading | pubmed-meshheading:8180658-... | lld:pubmed |
| pubmed-article:8180658 | pubmed:meshHeading | pubmed-meshheading:8180658-... | lld:pubmed |
| pubmed-article:8180658 | pubmed:meshHeading | pubmed-meshheading:8180658-... | lld:pubmed |
| pubmed-article:8180658 | pubmed:year | 1994 | lld:pubmed |
| pubmed-article:8180658 | pubmed:articleTitle | Analysis of amino acids by gas chromatography-flame ionization detection and gas chromatography-mass spectrometry: simultaneous derivatization of functional groups by an aqueous-phase chloroformate-mediated reaction. | lld:pubmed |
| pubmed-article:8180658 | pubmed:affiliation | Department of Chemistry, Michigan State University, East Lansing 48824. | lld:pubmed |
| pubmed-article:8180658 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:8180658 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
| pubmed-article:8180658 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:8180658 | lld:pubmed |
