One-step synthesis of novel 2,2'-bi(4,5-dihydro-1,3,4-thiadiazole) and 2,3-disubstituted 1,4-benzothiazine derivatives
- Author
- FARAG, A. M; SHAWALI, A. S; ALGHARIB, M. A; DAWOOD, K. M
Univ. Cairo, fac. sci., dep. chemistry, Giza, Egypt - Source
Tetrahedron (Oxford. Print). 1994, Vol 50, Num 17 ; VIII, 5091-5098 [9 p.] ; ref : 10 ref
- CODEN
- TETRAB
- ISSN
- 0040-4020
- Scientific domain
- Organic chemistry
- Publisher
- Elsevier, Oxford
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Keyword (fr)
- Acylation Acétique acide anhydride Aminothiol Chlorure acyle Composé benzénique Composé bicyclique Cycle 5 chaînons Hétérocycle soufre azote Nitreux acide Nitrosation Oxydation Potassium Thiocyanate Pyrolyse Thiourée 1,4-Benzothiazin-2-one(4-aryldiazényl) arylhydrazone 2,2p-Bi(1,3,4-thiadiazolyle-5,5p-dione)(4,4p-diaryl-4,4p,5,5p-tétrahydro) Benzoïque acide chlorure Benzènethiol(2-amino) Oxalohydrazonique acide(N,N -diaryl) dichlorure
- Keyword (en)
- Acylation Acetic acid,anhydride Aminothiol Acyl chloride Benzenic compound Bicyclic compound Five membered ring Sulfur nitrogen heterocycle Nitrous acid Nitrosation Oxidation Potassium Thiocyanates Pyrolysis Thiourea
- Keyword (es)
- Acilación Acético ácido,anhídrido Aminotiol Cloruro acilo Compuesto bencénico Compuesto bicíclico Ciclo 5 eslabones Heterociclo azufre nitrógeno Nitroso ácido Nitrosación Oxidación Potasio Tiocianato Pirólisis Tiourea
- Classification
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C06 Heterocyclic compounds / 001C03C06D Heterocyclic compounds with n hetero atom and also o and/or s, se, te hetero atoms
- Discipline
- Organic chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 4052621
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
10.1016/S0040-4020(01)90419-3 
https://dx.doi.org/10.1016/S0040-4020(01)90419-3
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