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kw.\*:("PHENOL(ALKYL-4 DI-T-BUTYL-2,6)")

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BASE-CATALYZED OXYGENATION OF TERT-BUTYLATED PHENOLS. I. REGIOSELECTIVITY IN THE BASE-CATALYZED OXYGENATION OF TERT-BUTYLPHENOLS.NISHINAGA A; ITAHARA T; SHIMIZU T et al.1978; J. AMER. CHEM. SOC.; U.S.A.; DA. 1978; VOL. 100; NO 6; PP. 1820-1825; BIBL. 33 REF.Article

RADICAL CATIONS OF 2,6-DI-TERT-BUTYL-4-ALKYLPHENOLS STUDIED BY ELECTRON SPIN RESONANCE SPECTROSCOPYNEMOTO F; TSUZUKI N; MUKAI K et al.1981; J. PHYS. CHEM.; ISSN 0022-3654; USA; DA. 1981; VOL. 85; NO 17; PP. 2450-2454; BIBL. DISSEM.Article

PHOTOLYSIS OF 2,6-DI-TERT-BUTYL-4-ALKYLPHENOLS WITH POLYHALOMETHANESWANG RHS.1972; J. ORG. CHEM.; U.S.A.; DA. 1972; VOL. 37; NO 17; PP. 2771-2774; BIBL. DISSEM.Serial Issue

Désalkylation des dérivés du di-tert-butyl-2,6 phénol en présence d'hétéropolyacidesKULIKOV, S. M; KOZHEVNIKOV, I. V; FOMINA, M. N et al.Kinetika i kataliz. 1986, Vol 27, Num 3, pp 750-753, issn 0453-8811Article

A NOVEL BASE-CATALYZED REARRANGEMENT OF P-PEROXYQUINOL ESTERS.NISHINAGA A; NAKAMURA K; YOSHIDA K et al.1977; CHEM. LETTERS; JAP.; DA. 1977; NO 3; PP. 303-306; BIBL. 14 REF.Article

ELEKTROCHEMISCHE OXIDATION. III: HERSTELLUNG VON CHINOLEN UND CHINOL-DERIVATEN DURCH ANODISCHE OXIDATION STERISCH GEHINDERTER PHENOLE = OXYDATION ELECTROCHIMIQUE. III. PREPARATION DE QUINOLS ET DE DERIVES DE QUINOLS PAR OXYDATION ANODIQUE DE PHENOLS EMPECHES STERIQUEMENTRIEKER A; DREHER EL; GEISEL H et al.1978; SYNTHESIS; DEU; DA. 1978; NO 11; PP. 851-855; BIBL. 27 REF.Article

ELEKTROCHEMISCHE OXIDATION. VII: SYNTHESE UND STRUKTUR VON 7-TERT-BUTYL-2-METHYLBENZOXAZOLEN = OXYDATION ELECTROCHIMIQUE. VII. SYNTHESE ET STRUCTURE DE T-BUTYL-7 METHYL-2 BENZOOXAZOLESDREHER EL; BRACHT J; MEDHAT EL MOBAYED et al.1982; CHEM. BER.; ISSN 0009-2940; DEU; DA. 1982; VOL. 115; NO 1; PP. 288-308; ABS. ENG; BIBL. 58 REF.Article

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