Deoxygenative vs. vicarious nucleophilic substitution of hydrogen in reactions of 1,2,4-triazine 4-oxides with α-halocarbanions

European Journal of Organic Chemistry

Volumn , Issue 8, 2002, Pages 1412-1416

  Kozhevnikov, Dmitry N ^a   Rusinov, Vladimir L ^a   Chupakhin, Oleg N ^a   Makosza, Mieczyslaw ^b   Rykowski, Andrzej ^c   Wolinska, Ewa ^c  

^a URAL FEDERAL UNIVERSITY   (Russian Federation)

^b POLISH ACADEMY OF SCIENCES   (Poland)

^c SIEDLCE UNIVERSITY OF NATURAL SCIENCES AND HUMANITIES   (Poland)

Author keywords

Aromatic substitution; C C coupling; Carbanions; Nitrogen heterocycles; Nucleophilic substitution

Indexed keywords

1,2,4 TRIAZINE 4 OXIDE; 5 SULFONYLCHLOROMETHYL 1,2,4 TRIAZINE; 5 TOSYLMETHYL 1,2,4 TRIAZINE 4 OXIDE; 6 PHENYL 1,2,4 TRIAZINE 4 OXIDE; 7 CHLORO 1 HYDROXY 3 PHENYL 7 (2 TOLYLSULFONYL) 1,4,5 TRIAZAHEPTA 1,3,6 TRIENE; 7 CHLORO 1 HYDROXY 3 PHENYL 7 (PHENYLSULFONYL) 1,4,5 TRIAZAHEPTA 1,3,6 TRIENE; ALPHA HALOCARBANION; ANION; BROMOMETHYL TOLYL SULFONE; HETEROCYCLIC COMPOUND; HYDROGEN; SULFONE DERIVATIVE; TRIAZINE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; LOW TEMPERATURE; OXIDATION REDUCTION REACTION; PROTON NUCLEAR MAGNETIC RESONANCE; REACTION ANALYSIS; ROOM TEMPERATURE; STOICHIOMETRY;

EID: 0036224575     PISSN: 1434193X     EISSN: None     Source Type: Journal    
DOI: 10.1002/1099-0690(200204)2002:8<1412::AID-EJOC1412>3.0.CO;2-9     Document Type: Article

References (17)