New Practical Synthesis of Indazoles via Condensation of o-Fluorobenzaldehydes and Their O-Methyloximes with Hydrazine
Author:
Affiliation:
1. GPRD Process Research and Development, Abbott Laboratories, North Chicago, Illinois 60064
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo0613784
Reference32 articles.
1. Potent cyclic urea HIV protease inhibitors with benzofused heterocycles as P2/P2′ groups
2. The recent impact of solid-phase synthesis on medicinally relevant benzoannelated nitrogen heterocycles
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