| pubmed-article:15200341 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:15200341 | lifeskim:mentions | umls-concept:C0162867 | lld:lifeskim |
| pubmed-article:15200341 | lifeskim:mentions | umls-concept:C0001992 | lld:lifeskim |
| pubmed-article:15200341 | lifeskim:mentions | umls-concept:C0030956 | lld:lifeskim |
| pubmed-article:15200341 | lifeskim:mentions | umls-concept:C0443286 | lld:lifeskim |
| pubmed-article:15200341 | lifeskim:mentions | umls-concept:C0439851 | lld:lifeskim |
| pubmed-article:15200341 | lifeskim:mentions | umls-concept:C0205250 | lld:lifeskim |
| pubmed-article:15200341 | lifeskim:mentions | umls-concept:C1552596 | lld:lifeskim |
| pubmed-article:15200341 | lifeskim:mentions | umls-concept:C0599956 | lld:lifeskim |
| pubmed-article:15200341 | lifeskim:mentions | umls-concept:C1947931 | lld:lifeskim |
| pubmed-article:15200341 | lifeskim:mentions | umls-concept:C0050452 | lld:lifeskim |
| pubmed-article:15200341 | lifeskim:mentions | umls-concept:C0761982 | lld:lifeskim |
| pubmed-article:15200341 | pubmed:issue | 13 | lld:pubmed |
| pubmed-article:15200341 | pubmed:dateCreated | 2004-6-17 | lld:pubmed |
| pubmed-article:15200341 | pubmed:abstractText | [reaction: see text] L-Proline-based small peptides have been developed as efficient catalysts for the asymmetric direct aldol reactions of hydroxyacetone with aldehydes. Chiral 1,4-diols 7, which are disfavored products in similar aldol reactions catalyzed by either aldolases or L-proline, were obtained in high yields and enantioselectivities of up to 96% ee with peptides 3 and 4 in aqueous media. | lld:pubmed |
| pubmed-article:15200341 | pubmed:language | eng | lld:pubmed |
| pubmed-article:15200341 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15200341 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:15200341 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15200341 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15200341 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15200341 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15200341 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15200341 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15200341 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15200341 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15200341 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15200341 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:15200341 | pubmed:month | Jun | lld:pubmed |
| pubmed-article:15200341 | pubmed:issn | 1523-7060 | lld:pubmed |
| pubmed-article:15200341 | pubmed:author | pubmed-author:GongLiu-ZhuLZ | lld:pubmed |
| pubmed-article:15200341 | pubmed:author | pubmed-author:MiAi-QiaoAQ | lld:pubmed |
| pubmed-article:15200341 | pubmed:author | pubmed-author:JiangYao-Zhon... | lld:pubmed |
| pubmed-article:15200341 | pubmed:author | pubmed-author:YangZhi-HuaZH | lld:pubmed |
| pubmed-article:15200341 | pubmed:author | pubmed-author:TangZhuoZ | lld:pubmed |
| pubmed-article:15200341 | pubmed:author | pubmed-author:CunLin-FengLF | lld:pubmed |
| pubmed-article:15200341 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:15200341 | pubmed:day | 24 | lld:pubmed |
| pubmed-article:15200341 | pubmed:volume | 6 | lld:pubmed |
| pubmed-article:15200341 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:15200341 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:15200341 | pubmed:pagination | 2285-7 | lld:pubmed |
| pubmed-article:15200341 | pubmed:dateRevised | 2006-11-15 | lld:pubmed |
| pubmed-article:15200341 | pubmed:meshHeading | pubmed-meshheading:15200341... | lld:pubmed |
| pubmed-article:15200341 | pubmed:meshHeading | pubmed-meshheading:15200341... | lld:pubmed |
| pubmed-article:15200341 | pubmed:meshHeading | pubmed-meshheading:15200341... | lld:pubmed |
| pubmed-article:15200341 | pubmed:meshHeading | pubmed-meshheading:15200341... | lld:pubmed |
| pubmed-article:15200341 | pubmed:meshHeading | pubmed-meshheading:15200341... | lld:pubmed |
| pubmed-article:15200341 | pubmed:meshHeading | pubmed-meshheading:15200341... | lld:pubmed |
| pubmed-article:15200341 | pubmed:meshHeading | pubmed-meshheading:15200341... | lld:pubmed |
| pubmed-article:15200341 | pubmed:meshHeading | pubmed-meshheading:15200341... | lld:pubmed |
| pubmed-article:15200341 | pubmed:meshHeading | pubmed-meshheading:15200341... | lld:pubmed |
| pubmed-article:15200341 | pubmed:year | 2004 | lld:pubmed |
| pubmed-article:15200341 | pubmed:articleTitle | Small peptides catalyze highly enantioselective direct aldol reactions of aldehydes with hydroxyacetone: unprecedented regiocontrol in aqueous media. | lld:pubmed |
| pubmed-article:15200341 | pubmed:affiliation | Key Laboratory for Asymmetric Synthesis and Chirotechnology of Sichuan Province and Union Laboratory of Asymmetric Synthesis, Chengdu Institute of Organic Chemistry, Chinese Academy of Sciences, Chengdu, 610041, China. | lld:pubmed |
| pubmed-article:15200341 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:15200341 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
