Synthesis of lanopylin B1
- Author
- SNIDER, Barry B1 ; JINGYE ZHOU1
[1] Department of Chemistry MS 015, Brandeis University, Waltham, Massachusetts 02454-9110, United States - Source
Journal of organic chemistry. 2005, Vol 70, Num 3, pp 1087-1088, 2 p
- 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)
- Alkylation Azide Enone Hétérocycle azote Phosphonate organique Pyrrole dérivé Réaction Horner Emmons Réaction Wittig Réaction aza-Wittig Réaction intramoléculaire Réaction transfert phase Synthèse chimique Toluène dérivé Heptadecanal Lanopyline B1 Pyrrole(3,4-dihydro-4-heptadécylidène-5-méthyl) Triphénylphosphine
- Keyword (en)
- Alkylation Organic azide Enone Nitrogen heterocycle Organic phosphonate Pyrrole derivatives Horner Emmons reaction Wittig reaction Aza-Wittig reaction Intramolecular reaction Phase transfer reaction Chemical synthesis Toluene derivatives
- Keyword (es)
- Alquilación Azida orgánica Enona Heterociclo nitrógeno Fosfonato orgánico Pirrol derivado Reacción Horner Emmons Reacción Wittig Reacción aza-Wittig Reacción intramolecular Reacción transferencia fase Síntesis química Tolueno derivado
- 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
- 16480515
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/jo048131w 
https://dx.doi.org/10.1021/jo048131w
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