Sequential Nitration/Hydrogenation Protocol for the Synthesis of Triaminophloroglucinol: Safe Generation and Use of an Explosive Intermediate under Continuous-Flow Conditions-Reference-Cited by-同舟云学术

Sequential Nitration/Hydrogenation Protocol for the Synthesis of Triaminophloroglucinol: Safe Generation and Use of an Explosive Intermediate under Continuous-Flow Conditions

Published:2014-06-17 Issue:11 Volume:18 Page:1360-1366
ISSN:1083-6160
Container-title:Organic Process Research & Development
language:en
Short-container-title:Org. Process Res. Dev.

Author:

Cantillo David¹,Damm Markus¹,Dallinger Doris¹,Bauser Marcus²,Berger Markus²,Kappe C. Oliver¹

Affiliation:

1. Institute of Chemistry, University of Graz, Heinrichstrasse 28, A-8010 Graz, Austria

2. Global Drug Discovery, Medicinal Chemistry, Bayer HealthCare, D-13353 Berlin, Germany

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/op5001435

Reference62 articles.

1. A rigid, cyclohexane-based polyamino-polyalcohol as a versatile building block for tailored chelating agents

2. O-Alkylated Derivatives of 1,3,5-Triamino-1,3,5-trideoxy-cis-inositol: Triamine Ligands with Unexpectedly High Affinity toward Divalent Transition- and d10-Metal Ions

3. Derivatives of 1,3,5-Triamino-1,3,5-trideoxy-cis-inositol as Versatile Pentadentate Ligands for Protein Labeling with Re-186/188. Prelabeling, Biodistribution, and X-ray Structural Studies

4. Chelation Therapies: A Chemical and Biochemical Perspective

5. Chelating Agents for Metal Intoxication

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