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Object |
contentType |
Journal Article|Research Support, N.I.H., Extramural|Research Support, Non-U.S. Gov't|Research Support, U.S. Gov't, P.H.S. |
endingPage |
3544 |
issn |
1523-7052 1523-7060 |
issueIdentifier |
20 |
pageRange |
3541-3544 |
publicationName |
Organic Letters |
startingPage |
3541 |
hasFundingAgency |
http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_b5ad88fdb9d8a30d34a9b7f844c05af4 |
isSupportedBy |
http://rdf.ncbi.nlm.nih.gov/pubchem/grant/MD5_911355c7a9c38a443cfb8822acdace36 |
bibliographicCitation |
Thayumanavan R, Tanaka F, Barbas III CF. Direct organocatalytic asymmetric aldol reactions of alpha-amino aldehydes: expedient syntheses of highly enantiomerically enriched anti-beta-hydroxy-alpha-amino acids. Org Lett. 2004 Sep 30;6(20):3541–4. doi: 10.1021/ol0485417. PMID: 15387543. |
creator |
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_df1e0dc6a142ee36e95a34a504b309af http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_df5d8d1f148a33cd5a2eb6f3c10a63c7 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_0a0782d317f0f02a5b738152283c8578 |
date |
2004-08-27-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
identifier |
https://doi.org/10.1021/ol0485417 https://pubmed.ncbi.nlm.nih.gov/15387543 |
isPartOf |
https://portal.issn.org/resource/ISSN/1523-7060 https://portal.issn.org/resource/ISSN/1523-7052 http://rdf.ncbi.nlm.nih.gov/pubchem/journal/21677 |
language |
English |
source |
https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/ |
title |
Direct Organocatalytic Asymmetric Aldol Reactions of α-Amino Aldehydes: Expedient Syntheses of Highly Enantiomerically Enriched anti-β-Hydroxy-α-amino Acids |
discusses |
http://id.nlm.nih.gov/mesh/M0000679 http://id.nlm.nih.gov/mesh/M0011226 http://id.nlm.nih.gov/mesh/M0000922 http://id.nlm.nih.gov/mesh/M0017693 |
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hasSubjectTerm |
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discussesAsDerivedByTextMining |
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID363 http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID145742 |