Jump to main content
US EPA
United States Environmental Protection Agency
Search
Search
Main menu
Environmental Topics
Laws & Regulations
About EPA
Health & Environmental Research Online (HERO)
Contact Us
Print
Feedback
Export to File
Search:
This record has one attached file:
Add More Files
Attach File(s):
Display Name for File*:
Save
Citation
Tags
HERO ID
7493358
Reference Type
Journal Article
Title
Specific synthesis of 1-substituted phenothiazines using carbon dioxide protection of the NH group during lithiation
Author(s)
Katritzky, AR; De Miguel, LMV; Rewcastle, GW
Year
1988
Is Peer Reviewed?
1
Journal
Synthesis
ISSN:
0039-7881
EISSN:
1437-210X
Publisher
Georg Thieme Verlag
Volume
1988
Issue
3
Page Numbers
215-217
Language
English
DOI
10.1055/s-1988-27515
Abstract
The lithiation of phenothiazine when protected as the lithium salt of its carbamate occurs exclusively at the C-1 carbon atom. Reaction of the lithiated species with a variety of electrophiles readily produced several new 1-substituted phenothiazines, as well as a number of known compounds in superior yield to existing methods. © 1988 Georg Thieme Verlag. All rights reserved.
Keywords
phenothiazine derivative; drug analysis; methodology; nonhuman; nuclear magnetic resonance
Tags
Other
•
Harmful Algal Blooms- Health Effects
April 2021 Literature Search
Scopus
Home
Learn about HERO
Using HERO
Search HERO
Projects in HERO
Risk Assessment
Transparency & Integrity