(PDF) On the Preparation of 1,2,5-Selenadiazolo

On the Preparation of 1,2,5-Selenadiazolo [3,4-E]indole and Its [3,4-F] and [3,4-G] Isomers Through the Batcho–Leimgruber Indole Synthesis

Arkivoc - United States

doi 10.3998/ark.5550190.0002.109

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November 16, 2001

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ARKAT USA, Inc.

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On the Preparation of 1,2,5-Selenadiazolo [3,4-E]indole and Its [3,4-F] and [3,4-G] Isomers Through the Batcho–Leimgruber Indole Synthesis

Arkivoc - United States

doi 10.3998/ark.5550190.0002.109

Full Text

Abstract

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Date

Authors

Publisher

Related search

Design and Theoretical Study of D–A–π–A Organic Sensitizers With [1,2,5]Thiadiazolo[3,4-C]pyridine, [1,2,5]Selenadiazolo[3,4-C]pyridine, and [1,2,5]Oxadiazolo[3,4-C]pyridineπComponent

Convenient Synthesis of Highly Functionalized, 3,4-Disubstituted Indole Building Blocks

1,2,5-Oxadiazolo[3,4-B]glycyrrhetinic Acid

New Organocatalytic Asymmetric Synthesis of Highly Substituted Chiral 2-Oxospiro-[Indole-3,4′- (1′,4′-Dihydropyridine)] Derivatives

The Synthesis of Trans-3,4-Bis-(3,4-Dihydroxyphenyl)pyrrolidine, a Novel DA1 Agonist.

Synthesis, Biological Evaluation and Modeling Studies of New Pyrido[3,4-B] Indole Derivatives as Broad-Spectrum Potent Anticancer Agents

Synthesis of 9-Ethyl[1,2,5]selenadiazolo[3,4-H]quinolones by the Application of Modified Gould-Jacobs Reaction to N-Ethyl-2,1,3-Benzoselenadiazol-4-Amine

Synthesis of 3,4-Methylenedioxyphenyl-Glyoxal

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