Regio-and stereospecific synthesis of β -sulfonamidodisulfides and β-sulfonamidosulfides from aziridines using tetrathiomolybdate as a sulfur transfer reagent
- Author
- SURESHKUMAR, Devarajulu1 ; GUNASUNDARI, Thanikachalam1 ; GANESH, Venkataraman1 ; CHANDRASEKARAN, Srinivasan1
[1] Department of Organic Chemistry, Indian Institute of Science, Bangalore 560012, Karnataka, India - Source
Journal of organic chemistry. 2007, Vol 72, Num 6, pp 2106-2117, 12 p ; ref : 26 ref
- 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)
- Acide Lewis Aziridine dérivé Composé cyclique Cycle 7 chaînons Disulfure organique Hétérocycle azote Milieu neutre Réaction tandem Régiosélectivité Stéréospécificité Sulfure organique Synthèse chimique Thiomolybdate
- Keyword (en)
- Lewis acid Aziridine derivatives Cyclic compound Seven membered ring Organic disulfide Nitrogen heterocycle Neutral medium Tandem reaction Regioselectivity Stereospecificity Organic sulfide Chemical synthesis Thiomolybdates
- Keyword (es)
- Acido Lewis Compuesto cíclico Ciclo 7 eslabones Disulfuro orgánico Heterociclo nitrógeno Medio neutro Reacción tándem Regioselectividad Estereoespecificidad Sulfuro orgánico Síntesis química Tiomolibdato
- 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
- 18669448
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/jo0624389 
https://dx.doi.org/10.1021/jo0624389
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