The syntheses of mono- and disubstituted phthalocyanines using a dithioimide
- Author
- LEZNOFF, C. C1 ; GREENBERG, S; BEN KHOUW; LEVER, A. B. P
[1] York univ., dep. chemistry, North York ON M3J 1P3, Canada - Source
Canadian journal of chemistry (Print). = Journal canadien de chimie. 1987, Vol 65, Num 8, pp 1705-1713 ; ref : 36 ref
- CODEN
- CJCHAG
- ISSN
- 0008-4042
- Scientific domain
- Chemistry; Crystallography; Atomic molecular physics
- Publisher
- National Research Council of Canada, Ottawa, ON
- Publication country
- Canada
- Document type
- Article
- Language
- English
- Keyword (fr)
- Acide carboximidique Alkylation Composé aromatique Composé bicyclique Composé polycyclique Condensation chimique Hétérocycle azote Imide Macrocycle Thioimide Isoindolinedithione-1,3(néopentyloxy-5) Phtalimide,diimine Phtalocyanine dérivé
- Keyword (en)
- Carboximidic acid Alkylation Aromatic compound Bicyclic compound Polycyclic compound Condensation reaction Nitrogen heterocycle Imide Macrocycle Thioimide
- Keyword (es)
- Acido carboximídico Alquilación Compuesto aromático Compuesto bicíclico Compuesto policíclico Condensación química Heterociclo nitrógeno Imida Macrociclo Tioimida
- 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
- 7550182
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
10.1139/v87-285 
https://dx.doi.org/10.1139/v87-285
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