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Reaction of 2,3-allenoates with TsNBr2 in the presence of base : A facile highly stereoselective synthesis of (1E,2E ) -3 -bromo -4 -oxo -N' -tosyl -2 -alkenoxylimidic acid ethyl esters

Author
RUWEI SHEN1 ; XIAN HUANG1 2
[1] Department of Chemistry, Zhejiang University (Xixi Campus), Hangzhou 310028, China
[2] State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai 200032, China
Source

Journal of organic chemistry. 2007, Vol 72, Num 10, pp 3961-3964, 4 p ; ref : 14 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 imidique Brome composé organique Composé allénique Composé éthylénique Cétone Electrophile Ester Mécanisme réaction Potassium carbonate Stéréosélectivité Synthèse chimique
Keyword (en)
Imidic acid Organic bromine compounds Allenic compound Ethylenic compound Ketone Electrophile Ester Reaction mechanism Potassium carbonate Stereoselectivity Chemical synthesis
Keyword (es)
Acido imídico Compuesto alénico Compuesto etilénico Cetona Electrófilo Ester Mecanismo reacción Potasio carbonato Estereoselectividad Síntesis química
Classification
Pascal
001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03B Reactivity and mechanisms / 001C03B02 Kinetics and mechanisms

Pascal
001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C02 Aliphatic compounds

Discipline
Organic chemistry
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
18747093

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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