Stereoselective total synthesis of bengamide E from glyceraldehyde acetonide and a nonracemic γ-alkoxy allylic stannane
- Author
- MARSHALL, J. A; LUKE, G. P
Univ. South Carolina, dep. chemistry biochemistry, Columbia SC 29208, United States - Source
Journal of organic chemistry. 1993, Vol 58, Num 23, pp 6229-6234
- CODEN
- JOCEAH
- ISSN
- 0022-3263
- Scientific domain
- Biochemistry, molecular biology, biophysics; Organic chemistry
- Publisher
- American Chemical Society, Washington, DC
- Publication country
- United States
- Document type
- Article
- Language
- English
- Keyword (fr)
- Aldéhyde Antimicrobien Antiparasitaire Carboxamide Composé allylique Cycle 7 chaînons Enol éther Hétérocycle azote Lactame Stannane organique Stéréosélectivité Synthèse totale Triol Azépane dérivé Furylique alcool(α-[2,2-diméthyl-1,3-dioxolan-4-yl]) Non-6-énoïque acide(2-méthoxy-8-méthyl-3,4,5-trihydroxy)-2-oxoazépan-3-ylamide Pent-1-ène(1-benzyloxyméthoxy-4-méthyl-3-tributylstannyl) Propionique acide(3-benzyloxy-3-formyl-2-méthoxy) ester méthyle
- Keyword (en)
- Aldehyde Antimicrobial agent Parasiticid Carboxamide Allylic compound Seven membered ring Enol ether Nitrogen heterocycle Lactam Organic stannane Stereoselectivity Total synthesis Triol
- Keyword (es)
- Aldehído Antimicrobiano Antiparasitario Carboxamida Compuesto alílico Ciclo 7 eslabones Enol eter Heterociclo nitrógeno Lactamo Estannano orgánico Estereoselectividad Síntesis total Triol
- 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
- 3766708
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
10.1021/jo00075a017 
https://dx.doi.org/10.1021/jo00075a017
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