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Regioselective nucleophilic opening of epoxides and aziridines under neutral conditions in the presence of β-cyclodextrin in water

Author
SRINIVAS, B1 ; PAVAN KUMAR, V1 ; SRIDHAR, R1 ; SURENDRA, K1 ; NAGESWAR, Y. V. D1 ; RAMA RAO, K1
[1] Organic Chemistry Division-I, Indian Institute of Chemical Technology, Hyderabad 500 007, India
Source

Journal of molecular catalysis. A, Chemical. 2007, Vol 261, Num 1, pp 1-5, 5 p ; ref : 47 ref

ISSN
1381-1169
Scientific domain
General chemistry, physical chemistry
Publisher
Elsevier, Amsterdam
Publication country
Netherlands
Document type
Article
Language
English
Author keyword
Epoxide N-Tosyl aziridines Sodium cyanide Supramolecular catalysis Water β-Amino alcohols β-Cyclodextrin β-Hydroxy nitrile
Keyword (fr)
Aminoalcool Aziridine dérivé Catalyse Cyanure Cyclodextrine Décyclisation Eau Epoxyde Nitrile Réaction catalytique Réaction nucléophile Régiosélectivité Sodium
Keyword (en)
Aminoalcohol Aziridine derivatives Catalysis Cyanides Cyclodextrin Ring cleavage Water Epoxide Nitrile Catalytic reaction Nucleophilic reaction Regioselectivity Sodium
Keyword (es)
Aminoalcohol Catálisis Cianuro Ciclodextrina Desciclización Agua Epóxido Nitrilo Reacción catalítica Reacción nucléofila Regioselectividad Sodio
Classification
Pascal
001 Exact sciences and technology / 001C Chemistry / 001C01 General and physical chemistry / 001C01A Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry / 001C01A03 Catalysis

Discipline
General chemistry and physical chemistry
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
18378772

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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