Synthesis of [2′-(N-Ethylamino)‎-5′-Alkyl]phenyl-5,6,7,8-Tetrahydroacridine-9-Carboxy-2-Sulfone Derivatives by the Proton-Catalyzed Rearrangement of Corresponding Sulfonamides

Joint Authors

Sharma, Anamika
Jain, Sonika
Sirohi, Reenu
Kishore, D.

Source

Organic Chemistry International

Issue

Vol. 2011, Issue 2011 (31 Dec. 2011), pp.1-5, 5 p.

Publisher

Hindawi Publishing Corporation

Publication Date

2012-01-11

Country of Publication

Egypt

No. of Pages

5

Main Subjects

Chemistry

Abstract EN

Synthesis of a new series of heteroaryl sulfones 6(a–f) in which the heteroaryl part is represented by acridine derivatives has been developed and reported here.

The key step of this transformation involves the proton-catalyzed rearrangement of the sulphonamide derivatives 5(a–f) to the corresponding sulfones 6(a–f).

American Psychological Association (APA)

Sharma, Anamika& Jain, Sonika& Sirohi, Reenu& Kishore, D.. 2012. Synthesis of [2′-(N-Ethylamino)-5′-Alkyl]phenyl-5,6,7,8-Tetrahydroacridine-9-Carboxy-2-Sulfone Derivatives by the Proton-Catalyzed Rearrangement of Corresponding Sulfonamides. Organic Chemistry International،Vol. 2011, no. 2011, pp.1-5.
https://search.emarefa.net/detail/BIM-485253

Modern Language Association (MLA)

Sharma, Anamika…[et al.]. Synthesis of [2′-(N-Ethylamino)-5′-Alkyl]phenyl-5,6,7,8-Tetrahydroacridine-9-Carboxy-2-Sulfone Derivatives by the Proton-Catalyzed Rearrangement of Corresponding Sulfonamides. Organic Chemistry International No. 2011 (2011), pp.1-5.
https://search.emarefa.net/detail/BIM-485253

American Medical Association (AMA)

Sharma, Anamika& Jain, Sonika& Sirohi, Reenu& Kishore, D.. Synthesis of [2′-(N-Ethylamino)-5′-Alkyl]phenyl-5,6,7,8-Tetrahydroacridine-9-Carboxy-2-Sulfone Derivatives by the Proton-Catalyzed Rearrangement of Corresponding Sulfonamides. Organic Chemistry International. 2012. Vol. 2011, no. 2011, pp.1-5.
https://search.emarefa.net/detail/BIM-485253

Data Type

Journal Articles

Language

English

Notes

Includes bibliographical references

Record ID

BIM-485253