Studies on the antitumor agent CC-1065: 1-phenylsulfonyl-1,3-butadiene ― An electrophilic equivalent to 1,3-butadiene for the synthesis of 3,31-bipyrroles
- Author
- HALAZY, S; MAGNUS, P
Indiana univ., dep. chemistry - Source
Tetrahedron letters. 1984, Vol 25, Num 14, pp 1421-1424 ; ref : 8 ref
- CODEN
- TELEAY
- ISSN
- 0040-4039
- Scientific domain
- Biochemistry, molecular biology, biophysics; Organic chemistry
- Publisher
- Elsevier, Oxford
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Keyword (fr)
- Addition Michaël Antibiotique CC1065 Anticancéreux Bipyrrolyle-3,3p carboxylique-2 acide(benzènesulfonyl-1p méthyl-5p) ester éthyle Bipyrrolyle-3,3p(benzènesulfonyl-1 mésylacétyl-2p méthyl-5) Bipyrrolyle-3,3p(dibenzènesulfonyl-1,4p méthyl-5) Bipyrrolyle-3,3p(dibenzènesulfonyl-1,4p éthyl-2p méthyl-5) Carbanion Composé diénique conjugué Cycle 5 chaînons Hétérocycle azote Isonitrile Pyrrole(benzènesulfonyl-1 benzènesulfonyl-2p vinyl-4 méthyl-2) Sodium Hydrure Sulfone(butadiène-1,3yl phényl) Sulfone(isocyano-1 propyl p-tolyl) Sulfone(isocyano-1 éthyl p-tolyl) Sulfone(isocyanométhyl p-tolyl)
- Keyword (en)
- Michael addition Antineoplastic agent Carbanion Conjugated dienic compound Five membered ring Nitrogen heterocycle Isocyanide Sodium Hydrides
- 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
- 9474164
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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