Chiral Salen-Aluminum Complexes as Catalysts for Enantioselective Aldol Reactions of Aldehydes and 5-Alkoxyoxazoles: An Efficient Approach to the Asymmetric Synthesis of syn and anti beta-Hydroxy-alpha-amino Acid Derivatives Financial support has been provided by the National Institutes of Health (GM 43912-11 and GM 33328-18).
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| Title: | Chiral Salen-Aluminum Complexes as Catalysts for Enantioselective Aldol Reactions of Aldehydes and 5-Alkoxyoxazoles: An Efficient Approach to the Asymmetric Synthesis of syn and anti beta-Hydroxy-alpha-amino Acid Derivatives Financial support has been provided by the National Institutes of Health (GM 43912-11 and GM 33328-18). |
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| Authors: | Evans DA; Department of Chemistry & Chemical Biology Harvard University, Cambridge, MA 02138 (USA)., Janey JM, Magomedov N, Tedrow JS |
| Source: | Angewandte Chemie (International ed. in English) [Angew Chem Int Ed Engl] 2001 May 18; Vol. 40 (10), pp. 1884-1888. |
| Publication Type: | Journal Article |
| Journal Info: | Publisher: Wiley-VCH Country of Publication: Germany NLM ID: 0370543 Publication Model: Print Cited Medium: Internet ISSN: 1521-3773 (Electronic) Linking ISSN: 14337851 NLM ISO Abbreviation: Angew Chem Int Ed Engl |
| Database: | MEDLINE Ultimate |
| FullText | Text: Availability: 0 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 11385662 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Chiral Salen-Aluminum Complexes as Catalysts for Enantioselective Aldol Reactions of Aldehydes and 5-Alkoxyoxazoles: An Efficient Approach to the Asymmetric Synthesis of syn and anti beta-Hydroxy-alpha-amino Acid Derivatives Financial support has been provided by the National Institutes of Health (GM 43912-11 and GM 33328-18). – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Evans+DA%22">Evans DA</searchLink>; Department of Chemistry & Chemical Biology Harvard University, Cambridge, MA 02138 (USA).<br /><searchLink fieldCode="AU" term="%22Janey+JM%22">Janey JM</searchLink><br /><searchLink fieldCode="AU" term="%22Magomedov+N%22">Magomedov N</searchLink><br /><searchLink fieldCode="AU" term="%22Tedrow+JS%22">Tedrow JS</searchLink> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%220370543%22">Angewandte Chemie (International ed. in English)</searchLink> [Angew Chem Int Ed Engl] 2001 May 18; Vol. 40 (10), pp. 1884-1888. – Name: TypePub Label: Publication Type Group: TypPub Data: Journal Article – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Wiley-VCH%22">Wiley-VCH </searchLink><i>Country of Publication: </i>Germany <i>NLM ID: </i>0370543 <i>Publication Model: </i>Print <i>Cited Medium: </i>Internet <i>ISSN: </i>1521-3773 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2214337851%22">14337851 </searchLink><i>NLM ISO Abbreviation: </i>Angew Chem Int Ed Engl |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=11385662 |
| RecordInfo | BibRecord: BibEntity: Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 1884 Titles: – TitleFull: Chiral Salen-Aluminum Complexes as Catalysts for Enantioselective Aldol Reactions of Aldehydes and 5-Alkoxyoxazoles: An Efficient Approach to the Asymmetric Synthesis of syn and anti beta-Hydroxy-alpha-amino Acid Derivatives Financial support has been provided by the National Institutes of Health (GM 43912-11 and GM 33328-18). Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Evans DA – PersonEntity: Name: NameFull: Janey JM – PersonEntity: Name: NameFull: Magomedov N – PersonEntity: Name: NameFull: Tedrow JS IsPartOfRelationships: – BibEntity: Dates: – D: 18 M: 05 Text: 2001 May 18 Type: published Y: 2001 Identifiers: – Type: issn-electronic Value: 1521-3773 Numbering: – Type: volume Value: 40 – Type: issue Value: 10 Titles: – TitleFull: Angewandte Chemie (International ed. in English) Type: main |
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