Synthesis of Na-Boc-5β-cyano-deformyl-E-geissoschizine: a potential synthon in the preparation of sarpagan and ajmalan ring systems
- Author
- JOKELA, R; HALONEN, M; LOUNASMAA, M
Tech. univ. Helsinki, lab. organic bioorganic chemistry, 02150 Espoo, Finland - Source
Heterocycles (Sendai). 1994, Vol 38, Num 1, pp 189-196
- CODEN
- HTCYAM
- ISSN
- 0385-5414
- Scientific domain
- Organic chemistry
- Publisher
- Elsevier, Oxford
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Keyword (fr)
- Aminonitrile Composé aromatique Composé tétracyclique Composé éthylénique Cyanhydratation Déplacement chimique Hétérocycle azote angulaire Nitrone Potassium Cyanure Spectre RMN Carbone 13 Indolo[2,3-a]quinolizine-2-acétique acide(12-t-butoxycarbonyl-3-éthylidène-1,2,3,4,6,7,12,12b-octahydro) ester éthyle 5-oxyde Indolo[2,3-a]quinolizine-2-acétique acide(12-t-butoxycarbonyl-6-cyano-3-éthylidène-1,2,3,4,6,7,12,12b-octahydro) ester éthyle 5-oxyde
- Keyword (en)
- Aminonitrile Aromatic compound Tetracyclic compound Ethylenic compound Hydrocyanation Chemical shift Angular nitrogen heterocycle Nitrone Potassium Cyanides NMR spectrum
- Keyword (es)
- Aminonitrilo Compuesto aromático Compuesto tetracíclico Compuesto etilénico Cianhidratación Desplazamiento químico Heterociclo nitrógeno angular Nitrona Potasio Cianuro Espectro de RMN
- Classification
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C06 Heterocyclic compounds / 001C03C06C Heterocyclic compounds with several n hetero atoms in the same ring, in separated rings or in fused rings
- Discipline
- Organic chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 3873123
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-93-6571 
https://dx.doi.org/10.3987/COM-93-6571
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