Nucleophilic para-fluorination of 4-alkylphenols by hypervalent iodine reagent and pyridinium polyhydrogen fluoride (PPHF) a novel route to 4-fluorocyclohexa-2,5-dienones-Reference-Cited by-同舟云学术

Nucleophilic para-fluorination of 4-alkylphenols by hypervalent iodine reagent and pyridinium polyhydrogen fluoride (PPHF) a novel route to 4-fluorocyclohexa-2,5-dienones

Published:1994-04 Issue:16 Volume:35 Page:2541-2544
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Karam Omar,Jacquesy Jean-Claude,Jouannetaud Marie-Paule

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference22 articles.

1. Studies aiming at the synthesis of morphine II

2. Phenolic oxidation with (diacetoxyiodo)benzene

3. Phenolic oxidative coupling with hypervalent organo iodine compound (diacetoxyiodo) benzene

4. Studies on the synthesis of Stemona alkaloids; stereoselective preparation of the hydroindole ring system by oxidative cyclization of tyrosine

5. Total synthesis of discorhabdin C: a general aza spiro dienone formation from O-silylated phenol derivatives using a hypervalent iodine reagent

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