au.\*:("MUTHARD JL")
Results 1 to 5 of 5
Selection :
LONG-RANGE ELECTRONIC TRANSMISSION IN CONFORMATIONALLY RIGID ALPHA -DIKETONESBARTETZKO R; GLEITER R; MUTHARD JL et al.1978; J. AMER. CHEM. SOC.; USA; DA. 1978; VOL. 100; NO 18; PP. 5589-5594; BIBL. 25 REF.Article
C16-HEXAQUINACENE.PAQUETTE LA; SNOW RA; MUTHARD JL et al.1978; J. AMER. CHEM. SOC.; U.S.A.; DA. 1978; VOL. 100; NO 5; PP. 1600-1602; BIBL. 19 REF.Article
TOPOLOGICALLY SPHERICAL MOLECULES. AN EFFICIENT SYNTHESIS OF C16-HEXAQUINACENE AND ITS LACK OF NEUTRAL HOMOAROMATIC CHARACTERPAQUETTE LA; SNOW RA; MUTHARD JL et al.1979; J. AMER. CHEM. SOC.; USA; DA. 1979; VOL. 101; NO 23; PP. 6991-6996; BIBL. 34 REF.Article
QUANTITATIVE ASSESSMENT OF PP-O OVERLAP IN A TOPOLOGICALLY CONVEX TRIENE-ELECTRONIC AND CRYSTAL STRUCTURE ANALYSIS OF C16-HEXAQUINACENECHRISTOPH GG; MUTHARD JL; PAQUETTE LA et al.1978; J. AMER. CHEM. SOC.; USA; DA. 1978; VOL. 100; NO 24; PP. 7782-7784; BIBL. 18 REF.Article
TOPOLOGICALLY SPHERICAL MOLECULES. SYNTHESIS OF A PAIR OF C2-SYMMETRIC HEXAQUINANE DILACTONES AND INSIGHTS INTO THEIR CHEMICAL REACTIVITY. AN EFFICIENT PI -MEDIATED 1,6-DICARBONYL REDUCTIONPAQUETTE LA; WYVRATT MJ; SCHALLNER O et al.1979; J. ORG. CHEM.; USA; DA. 1979; VOL. 44; NO 21; PP. 3616-3630; BIBL. 58 REF.Article