Stereoselective synthesis of (±)-5-(1-benzyloxyethyl)-6-(2-tert-butyldiphenyloxyethyl)-2-piperidinone: a formal total synthesis of thienamycin
- Author
- TANIMORI, S; NIKI, T; MINGQI HE; NAKAYAMA, M
Univ. Osaka prefecture, coll. agriculture, dep. agricultural chemistry, Sakai Osaka 593, Japan - Source
Heterocycles (Sendai). 1994, Vol 38, Num 7, pp 1533-1540 ; ref : 7 ref
- CODEN
- HTCYAM
- ISSN
- 0385-5414
- Scientific domain
- Organic chemistry
- Publisher
- Elsevier, Oxford
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Keyword (fr)
- Acide Lewis Composé bicyclique Composé monocyclique Cycle 6 chaînons Cétoester Ether Hétérocycle azote Méthanol Pipéridine dérivé Racémique Bicyclo[3.1.0]hexane-1-carboxylique acide(6-méthyl-2-oxo) ester méthyle Borane(trifluoro)-éthyle éther Cyclopentanecarboxylique acide(2-[1-méthoxyéthyl]-5-oxo) ester méthyle Pipéridin-2-one(5-[1-benzyloxyéthyl]-6-[2-(t-butyldiphénylsiloxy)éthyl]) p-Toluènesulfonique acide
- Keyword (en)
- Lewis acid Bicyclic compound Monocyclic compound Six membered ring Ketoester Ether Nitrogen heterocycle Methanol Piperidine derivatives Racemate
- Keyword (es)
- Acido Lewis Compuesto bicíclico Compuesto monocíclico Ciclo 6 eslabones Cetoester Eter Heterociclo nitrógeno Metanol Piperidina derivado Racémico
- Classification
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C06 Heterocyclic compounds / 001C03C06B Heterocyclic compounds with only one n hetero atom and condensed derivatives
- Discipline
- Organic chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 4171010
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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DOI
10.3987/COM-94-6714 
https://dx.doi.org/10.3987/COM-94-6714
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