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Addition-elimination strategy for asymmetric induction : a chiral sulfoxide as a leaving group

Author
FUJI, K1 ; NODE, M; ABE, H; ITOH, A; MASAKI, Y; SHIRO, M
[1] Kyoto univ., inst. chemical res., Kyoto 611, Japan
Source

Tetrahedron letters. 1990, Vol 31, Num 17, pp 2419-2422 ; ref : 11 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 chimique Composé benzénique Composé monocyclique Composé nitro Composé saturé Elimination Enolate Exces énantiomère Hétérocycle azote Induction asymétrique Lactame Sel organique Sulfoxyde Pipéridone-2(méthyl-«1» nitro-«2p» cyclohexène-«1p» yl-«3») Pyridinolate-2(méthyl-«1» tétrahydro-«1,4,5,6») Sulfoxyde(nitro-2 cyclohexène-«1»yl phényl-«2» propyl)
Keyword (en)
Addition reaction Benzenic compound Monocyclic compound Nitro compound Saturated compound Elimination Enolate Enantiomeric excess Nitrogen heterocycle Asymmetric induction Lactam Organic salt Sulfoxide
Keyword (es)
Adición química Compuesto bencénico Compuesto monocíclico Compuesto nitro Compuesto saturado Eliminación Enolato Exceso enantiómero Heterociclo nitrógeno Inducción asimétrica Lactamo Sal orgánica Sulfóxido
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
6889256

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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