1,1',2,2'-TETRATHIAFULVALENE. II: THIENO (3,2-B) THIOPHENE AUS 1,2-DITHIOL-VERBINDUNGEN: 3H-1,2-DITHIOL-3-YLIDENE (1,2-DITHIOL-3-CARBONE) ALS MUTMASSLICHE ZWISCHENSTUFEN
- Other title
- TETRATHIA-1,1',2,2' FULVALENES. II: THIENO (3,2-B) THIOPHENE A PARTIR DE COMPOSES DU DITHIOLE-1,2: 3H-DITHIOLE-1,2YLIDENES-3 (CARBENA-3 DITHIOLES-1,2) COMME INTERMEDIAIRES POSSIBLES (fr)
- Author
- BEHRINGER H; MEINETSBERGER E
UNIV. MUENCHEN, INST. ORGAN. CHEM./MUENCHEN 8000/DEU - Source
- LIEBIGS ANN. CHEM.; ISSN 0170-2041; DEU; DA. 1981; NO 10; PP. 1729-1750; ABS. ENG; BIBL. 42 REF.
- Document type
- Article
- Language
- German
- Keyword (fr)
- CARBENE HETEROCYCLE SOUFRE COMPOSE BICYCLIQUE CYCLE 5 CHAINONS PREPARATION REACTION CHIMIQUE DEPROTONATION COMPOSE TRICYCLIQUE SPECTRE RMN PYROLYSE DESULFURATION SPECTRE UV SPECTRE IR SPECTRE MASSE CARBENA-3DITHIOLE-1,2(DIPHENYL-4,5)!FIN THIENO THIOPHENE DERIVE!FIN DITHIOLE-1,2THIONE-3(METHYL-4 PHENYL-5)!FIN BENZODITHIOLE-1,2 DERIVE!FIN DITHIOLE-1,2YLIUM COMPOSE!ENT BENZOTHIOPYRANNE-1(DIPHENYL-2,3 EPITHIO-4,8 HEXAHYDRO-4A,5,6,7,8,8A MORPHOLINO-8A)!FIN DITHIOLE-1,2ONE-3(PHENYL-5) TOSYLHYDRAZONE!ENT DITHIETANNE-1,3(DIPHENACYLIDENE-2,4)!ENT MORPHOLINE(CYCLOHEXENE-1P YL-4)!ENT HYDROGENE 1 CARBONE 13 CHIMIE ORGANIQUE
- Keyword (en)
- CARBENE SULFUR HETEROCYCLE BICYCLIC COMPOUND FIVE MEMBERED RING PREPARATION CHEMICAL REACTION DEPROTONATION TRICYCLIC COMPOUND NMR SPECTRUM PYROLYSIS DESULFURIZATION ULTRAVIOLET SPECTRUM INFRARED SPECTRUM MASS SPECTRUM ORGANIC CHEMISTRY
- Keyword (es)
- QUIMICA ORGANICA
- Classification
- Discipline
- Organic chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- PASCAL82X0015967
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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Istex access
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Europe PubMed Central access
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