Efficient One-Pot Synthesis of Spirooxindole Derivatives by Ethylenediamine Diacetate Catalyzed Reactions in Water

Title
Efficient One-Pot Synthesis of Spirooxindole Derivatives by Ethylenediamine Diacetate Catalyzed Reactions in Water
Author(s)
이용록갈라스리하리[갈라스리하리]
Keywords
MAMMALIAN-CELL CYCLE; PYRANOCHALCONE NATURAL-PRODUCTS; PUMMERER REACTION CHEMISTRY; CONCISE TOTAL-SYNTHESIS; DIELS-ALDER REACTIONS; ASPERGILLUS-FUMIGATUS; ASYMMETRIC-SYNTHESIS; CLAISEN REARRANGEMENT; TRYPROSTATIN-B; AQUEOUS-MEDIA
Issue Date
201002
Publisher
GEORG THIEME VERLAG KG
Citation
SYNTHESIS-STUTTGART, no.3, pp.453 - 464
Abstract
A simple and efficient one-pot synthetic approach was used for the preparation of biologically interesting spirooxindole derivatives by means of three-component reactions of isatins, malononitrile, and 1,3-dicarbonyl compounds catalyzed by ethylenediamine diacetate (EDDA) in an aqueous medium. This method is of great value because of its environmentally benign character, high yield, and easy handling.
URI
http://hdl.handle.net/YU.REPOSITORY/22907http://dx.doi.org/10.1055/s-0029-1217116
ISSN
0039-7881
Appears in Collections:
공과대학 > 화학공학부 > Articles
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