Convenient Transformation of Carbonyl Compounds Via Their Hydrazones into Gem-Difluoro Compounds With N-Bromosuccinimide/pyridinium Poly(Hydrogen Fluoride) Or Poly-4-Vinyl-Pyridinium Poly(Hydrogen Fluoride)

Author

G. K. Surya Prakash
V. Prakash Reddy, Missouri University of Science and TechnologyFollow
Xing Ya Li
George A. Olah

Abstract

In situ generated bromine monofluoride (BrF) from N-bromosuccinimide/pyridinium poly(hydrogen fluoride) or poly-4-vinylpyridinium poly(hydrogen fluoride) reacts with hydrazones to give the corresponding gem-difluoro compounds (8 examples) in satisfactory yield.

Recommended Citation

G. K. Surya Prakash et al., "Convenient Transformation of Carbonyl Compounds Via Their Hydrazones into Gem-Difluoro Compounds With N-Bromosuccinimide/pyridinium Poly(Hydrogen Fluoride) Or Poly-4-Vinyl-Pyridinium Poly(Hydrogen Fluoride)," Synlett, vol. 1990, no. 10, pp. 594 - 596, Thieme Gruppe, Oct 1990.

The definitive version is available at https://doi.org/10.1055/s-1990-21177

Department(s)

Chemistry

Comments

Office of Naval Research, Grant None

International Standard Serial Number (ISSN)

1437-2096; 0936-5214

Document Type

Article - Journal

Document Version

Citation

File Type

text

Language(s)

English

Rights

© 2024 Thieme Gruppe, All rights reserved.

Publication Date

01 Oct 1990