| pubmed-article:10399017 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:10399017 | lifeskim:mentions | umls-concept:C0001128 | lld:lifeskim |
| pubmed-article:10399017 | lifeskim:mentions | umls-concept:C1545588 | lld:lifeskim |
| pubmed-article:10399017 | lifeskim:mentions | umls-concept:C0220781 | lld:lifeskim |
| pubmed-article:10399017 | lifeskim:mentions | umls-concept:C0679199 | lld:lifeskim |
| pubmed-article:10399017 | lifeskim:mentions | umls-concept:C1883254 | lld:lifeskim |
| pubmed-article:10399017 | lifeskim:mentions | umls-concept:C1879547 | lld:lifeskim |
| pubmed-article:10399017 | pubmed:issue | 3-4 | lld:pubmed |
| pubmed-article:10399017 | pubmed:dateCreated | 1999-8-23 | lld:pubmed |
| pubmed-article:10399017 | pubmed:abstractText | A new method for the preparation of N-methylamino acids and some of their derivatives starting from hexafluoroacetone protected amino acids is described. The new concept results in saving of steps compared to conventional protection/activation techniques. Protection and deprotection proceed without recemization. | lld:pubmed |
| pubmed-article:10399017 | pubmed:language | eng | lld:pubmed |
| pubmed-article:10399017 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:10399017 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:10399017 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:10399017 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:10399017 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:10399017 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:10399017 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:10399017 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:10399017 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:10399017 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:10399017 | pubmed:issn | 0939-4451 | lld:pubmed |
| pubmed-article:10399017 | pubmed:author | pubmed-author:BurgerKK | lld:pubmed |
| pubmed-article:10399017 | pubmed:author | pubmed-author:SchedelHH | lld:pubmed |
| pubmed-article:10399017 | pubmed:author | pubmed-author:SpenglerJJ | lld:pubmed |
| pubmed-article:10399017 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:10399017 | pubmed:volume | 16 | lld:pubmed |
| pubmed-article:10399017 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:10399017 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:10399017 | pubmed:pagination | 287-95 | lld:pubmed |
| pubmed-article:10399017 | pubmed:dateRevised | 2006-11-15 | lld:pubmed |
| pubmed-article:10399017 | pubmed:meshHeading | pubmed-meshheading:10399017... | lld:pubmed |
| pubmed-article:10399017 | pubmed:meshHeading | pubmed-meshheading:10399017... | lld:pubmed |
| pubmed-article:10399017 | pubmed:meshHeading | pubmed-meshheading:10399017... | lld:pubmed |
| pubmed-article:10399017 | pubmed:meshHeading | pubmed-meshheading:10399017... | lld:pubmed |
| pubmed-article:10399017 | pubmed:meshHeading | pubmed-meshheading:10399017... | lld:pubmed |
| pubmed-article:10399017 | pubmed:meshHeading | pubmed-meshheading:10399017... | lld:pubmed |
| pubmed-article:10399017 | pubmed:year | 1999 | lld:pubmed |
| pubmed-article:10399017 | pubmed:articleTitle | A new protection/activation strategy for the synthesis of naturally occurring and non-natural alpha-N-alkylamino acids. | lld:pubmed |
| pubmed-article:10399017 | pubmed:affiliation | Institut für Organische Chemie, Universität Leipzig, Federal Republic of Germany. burger@organik.orgchem.uni-leipzig.de | lld:pubmed |
| pubmed-article:10399017 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:10399017 | pubmed:publicationType | Review | lld:pubmed |
| pubmed-article:10399017 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
