Improved purification of C₆₀ and formation of σ- and π-homoaromatic methano-bridged fullerenes by reaction with alkyl diazoacetatesISAACS, L; WEHRSIG, A; DIEDERICH, F et al.Helvetica chimica acta. 1993, Vol 76, Num 3, pp 1231-1250, issn 0018-019XArticle

UEBERGANGSMETALL-METHYLEN-KOMPLEXE. VI: ZUR IRREVERSIBLEN MU -METHYLEN/CARBONYL-ISOMERIE ZWEIKERNIGER COBALT-KOMPLEXE MIT BIFUNKTIONELLEN METHYLEN-LIGANDEN = COMPLEXE METHYLENE-METAL DE TRANSITION. VI. ISOMERISATION IRREVERSIBLE MU -METHYLENE/CARBONYLE DES COMPLEXES DE CO DINUCLEAIRES AVEC DES COORDINATS ORGANIQUES BIFONCTIONNELSHERRMANN WA; SCHWEIZER I.1978; Z. NATURFORSCH., B; DEU; DA. 1978; VOL. 33; NO 10; PP. 1128-1135; ABS. ENG; BIBL. 26 REF.Article

SYNTHETIC SCOPE OF THE TRIETHYLOXONIUM ION CATALYZED HOMOLOGATION OF KETONES WITH DIAZOACETIC ESTERS.MOCK WL; HARTMAN ME.1977; J. ORG. CHEM.; U.S.A.; DA. 1977; VOL. 42; NO 3; PP. 459-465; BIBL. 27 REF.Article

Asymmetric cyclopropanation of E-olefins using a copper complex of an optically active bipyridine as a catalystITO, K; KATSUKI, T.Synlett. 1993, Num 9, pp 638-640, issn 0936-5214Article

SYNTHESIS AND X-RAY CRYSTAL STRUCTURE OF 1,5-BIS(ACETOXYMETHYL)-TRICYCLO (2.1.0.0^2,5) PENTAN-3-ONEIRNGARTINGER H; GOLDMANN A; SCHAPPERT R et al.1981; J. CHEM. SOC., CHEM. COMMUN.; ISSN 0022-4936; GBR; DA. 1981; NO 10; PP. 455-456; BIBL. 7 REF.Article

Cyclopropanation of styrene with diazoacetates catalyzed by copper and rhodium complexes of new chiral 2,2' :6', 2-terpyridines derived from natural occurring compoundsCHELUCCI, Giorgio; SABA, Antonio; SOCCOLINI, Franco et al.Journal of molecular catalysis. A, Chemical. 2002, Vol 178, Num 1-2, pp 27-33, issn 1381-1169Article

Conformationally restricted P₁-P₁' transition state analogues. Synthesis of 1(R), 3(R) [1(S), 2(S)] and 1(S), 3(S) [1(S), 2(S)] 3-[3-cyclohexyl-2-[(BOC)amino]-1-hydroxypropyl]-2,2-dimethylcyclopropane carboxylic acidsMELNICK, M. J; BISAHA, S. N; GAMMILL, R. B et al.Tetrahedron letters. 1990, Vol 31, Num 7, pp 961-964, issn 0040-4039Article

Diazoverbindungen. LXV: Isomerisierungen in System 4-Diazo-1-buten/2.3-Diazabicyclo[3.1.0]hex-2-en/1.4-Dihydropyridazin = Composés diazo. LXV: Isomérisations dans le système diazo-4 butène-1/diaza-2,3bicyclo [3.1.0] hexène-2/dihydro-1,4 pyridazine = Diazo compounds. LXV: Isomerization reactions in the system 4-diazo-1-butene/2,3-diazabicyclo [3.1.0] hex-2-ene/1,4-dihydropyridazineHEYDT, H; BREINER, H.-W; HELL, V et al.Zeitschrift für Naturforschung. Teil b, Anorganische Chemie, organische Chemie. 1987, Vol 42, Num 2, pp 210-216, issn 0340-5087Article