au.\*:("DUTHALER RO")
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CONSTRUCTION OF HIGHLY SUBSTITUTED NITROAROMATIC SYSTEMS BY CYCLOCONDENSATION. I: SYNTHESIS OF 4-NITRO-3-OXOBUTYRATEDUTHALER RO.1983; HELVETICA CHIMICA ACTA; ISSN 0018-019X; CHE; DA. 1983; VOL. 66; NO 5; PP. 1475-1492; BIBL. 38 REF.Article
SYNTHESIS OF OPTICALLY PURE COMPOUNDS BY ENANTIOTOPICALLY DIFFERENTIATING MONOACETALIZATION OF PROCHIRAL DIKETONESDUTHALER RO; MAIENFISCH P.1982; HELV. CHIM. ACTA; ISSN 0018-019X; CHE; DA. 1982; VOL. 65; NO 3; PP. 635-653; BIBL. 35 REF.Article
EFFECTS OF SOLVENT, PROTONATION, AND N-ALKYLATION ON THE 15N CHEMICAL SHIFTS OF PYRIDINE AND RELATED COMPOUNDSDUTHALER RO; ROBERTS JD.1978; J. AMER. CHEM. SOC.; USA; DA. 1978; VOL. 100; NO 16; PP. 4969-4973; BIBL. 17 REF.Article
STERIC AND ELECTRONIC EFFECTS ON 15N CHEMICAL SHIFTS OF SATURATED ALIPHATIC AMINES AND THEIR HYDROCHLORIDES.DUTHALER RO; ROBERTS JD.1978; J. AMER. CHEM. SOC.; USA; DA. 1978; VOL. 100; NO 12; PP. 3889-3895; BIBL. 12 REF.Article
2-OXO-9** (C(3))-HYDROXY- UND 2-OXO-9** (C(7))-HYDROXY-BICYCLO (3.3.1) NONAN = OXO-2 HYDROXY-9** (C(3)) ET OXO-2 HYDROXY-9** (C(7)) BICYCLO (3.3.1) NONANESDUTHALER RO; GANTER C.1975; HELV. CHIM. ACTA; SUISSE; DA. 1975; VOL. 58; NO 5; PP. 1366-1374; ABS. ANGL.; BIBL. 5 REF.Article
15N AND 13C NUCLEAR MAGNETIC RESONANCE SPECTRA OF DIAZO AND DIAZONIUM COMPOUNDSDUTHALER RO; FORSTER HG; ROBERTS JD et al.1978; J. AMER. CHEM. SOC.; USA; DA. 1978; VOL. 100; NO 16; PP. 4974-4979; BIBL. 41 REF.Article
PHOTOCHEMISCHE REAKTIONEN. LXXXVI. ZUR PHOTOLYSE VON BICYCLO (3.3.1) NONAN-2-ON = REACTIONS PHOTOCHIMIQUES. LXXXVI. PHOTOLYSE DU BICYCLO (3.3.1) NONANONE-2DUTHALER RO; STINGELIN SCHMID RS; GANTER C et al.1976; HELV. CHIM. ACTA; SUISSE; DA. 1976; VOL. 59; NO 1; PP. 307-335; ABS. ANGL.; BIBL. 41 REF.Article
SUBSTITUIERTE 9-OXABICYCLO (4.2.1)- UND 9-OXABICYCLO (3.3.1) NONANE. IV. ENDO, ENDO-2,5-DIHYDROXY-9-OXABICYCLO (4.2.1) NONAN, ENDO ENDO-, ENDO, EXO- UND EXO, EXO-2,6-DIHYDROXY-SORVIE ENDO-, EXO-2,7-DIHYDROXY-9-OXABICYCLO (3.3.1) NONAN; DARSTELLUNG UND UMWANDLUNGSPRODUKTE = OXA-9 BICYCLO (4.2.1)- ET OXA-9 BICYCLO (3.3.1) NONANES SUBSTITUES. IV. ENDO, ENDO- DIHYDROXY-2,5 OXA-9 BICYCLO (4.2.1) NONANE, ENDO, ENDO-, ENDO, EXO- ET EXO-EXO- DIHYDROXY-2,6 ET AUSSI ENDO-EXO-DIHYDROXY-2,7 OXA-9 BICYCLO (3.3.1) NONANES; PREPARATION ET PRODUITS DE TRANSFORMATIONDUTHALER RO; WICKER K; ACKERMANN P et al.1972; HELV. CHIM. ACTA; SUISSE; DA. 1972; VOL. 55; NO 5; PP. 1809-1828; ABS. ANGL.; BIBL. 20 REF.Serial Issue
