A simple procedure for the solid phase synthesis of unsymmetrically functionalised diamides from symmetric diacids

Tipo de material: Texto

TextoSeries ; Tetrahedron Letters, 40(2), p.235-238, 1996Trabajos contenidos:

Wahhab, A
Leban, J

Recursos en línea:

Para ver el documento ingresa a Google con tu cuenta: @cicy.edu.mx

Resumen: The solid phase synthesis of unsymmetrically substituted diamides from symmetric dicarboxylic acids is described. The process was conducted following these steps: (1)preactivation of the dicarboxylic acid with BOP, (2)addition to amine resin, (3)reaction with a second amine, and (4)TFA cleavage to afford the desired diamide. Most of the unsymmetric diamides were obtained in >80

Tags from this library: No tags from this library for this title. Log in to add tags.

Average rating: 0.0 (0 votes)

Holdings
Item type	Current library	Collection	Call number	Status	Date due	Barcode
Documentos solicitados	CICY Documento préstamo interbibliotecario	Ref1	B-7684 (Browse shelf(Opens below))	Available

Browsing CICY shelves, Shelving location: Documento préstamo interbibliotecario, Collection: Ref1 Close shelf browser (Hides shelf browser)

Previous	No cover image available	No cover image available	No cover image available	No cover image available	No cover image available	No cover image available	No cover image available	Next
Previous	B-7681 New illudane sesquiterpenes from the basidiomycete Clitocybe rivulosa HKI 0273	B-7682 Symmetric Building Blocks and Combinatorial Functional Group Transformation as Versatile Strategies in Combinatorial Chemistry	B-7683 Infrared Spectroscopy in Solid-Phase Synthesis	B-7684 A simple procedure for the solid phase synthesis of unsymmetrically functionalised diamides from symmetric diacids	B-7685 Electrochemical Behavior of Single-Carbon Organic Compounds on a Composite Nafion-Polyaniline-Palladium Particle Electrode in Acid Solutions	B-7686 Aqueous pore structure and proton dynamics in solvated Nafion membranes	B-7687 The Chromosomal Basis of Somaclonal Variation	Next

The solid phase synthesis of unsymmetrically substituted diamides from symmetric dicarboxylic acids is described. The process was conducted following these steps: (1)preactivation of the dicarboxylic acid with BOP, (2)addition to amine resin, (3)reaction with a second amine, and (4)TFA cleavage to afford the desired diamide. Most of the unsymmetric diamides were obtained in >80

There are no comments on this title.

to post a comment.