A Novel, One-Step Palladium and Phenylsilane Activated Amidation from Allyl Ester on Solid Support

Joint Authors

Lawrence, R. Michael
Ruan, Zheming
Cooper, Christopher B.
Van Kirk, Katy

Source

Research Letters in Organic Chemistry

Issue

Vol. 2008, Issue 2008 (31 Dec. 2008), pp.1-4, 4 p.

Publisher

Hindawi Publishing Corporation

Publication Date

2008-09-16

Country of Publication

Egypt

No. of Pages

4

Main Subjects

Chemistry

Abstract EN

The direct conversion of solid-supported carboxylic acid allyl esters to carboxamides through the use of phenylsilane and catalytic Pd(PPh3)4 under mild reaction conditions is reported.

The use of this methodology for the generation of a 48 compound solid-phase array is described herein.

American Psychological Association (APA)

Ruan, Zheming& Van Kirk, Katy& Cooper, Christopher B.& Lawrence, R. Michael. 2008. A Novel, One-Step Palladium and Phenylsilane Activated Amidation from Allyl Ester on Solid Support. Research Letters in Organic Chemistry،Vol. 2008, no. 2008, pp.1-4.
https://search.emarefa.net/detail/BIM-491328

Modern Language Association (MLA)

Ruan, Zheming…[et al.]. A Novel, One-Step Palladium and Phenylsilane Activated Amidation from Allyl Ester on Solid Support. Research Letters in Organic Chemistry No. 2008 (2008), pp.1-4.
https://search.emarefa.net/detail/BIM-491328

American Medical Association (AMA)

Ruan, Zheming& Van Kirk, Katy& Cooper, Christopher B.& Lawrence, R. Michael. A Novel, One-Step Palladium and Phenylsilane Activated Amidation from Allyl Ester on Solid Support. Research Letters in Organic Chemistry. 2008. Vol. 2008, no. 2008, pp.1-4.
https://search.emarefa.net/detail/BIM-491328

Data Type

Journal Articles

Language

English

Notes

Includes bibliographical references

Record ID

BIM-491328