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Results: 1-14 |
Results: 14
First efficient synthesis of chlorogenic acid
Authors: Sefkow, M
Citation: M. Sefkow, First efficient synthesis of chlorogenic acid, EUR J ORG C, (6), 2001, pp. 1137-1141
First efficient syntheses of 1-, 4-, and 5-caffeoylquinic acid
Authors: Sefkow, M Kelling, A Schilde, U
Citation: M. Sefkow et al., First efficient syntheses of 1-, 4-, and 5-caffeoylquinic acid, EUR J ORG C, (14), 2001, pp. 2735-2742
A short synthesis of biologically active lignan analogues (pg 331, 2001)
Authors: Kamlage, S Sefkow, M Zobel, BL Peter, MG
Citation: S. Kamlage et al., A short synthesis of biologically active lignan analogues (pg 331, 2001), CHEM COMMUN, (6), 2001, pp. 507-507
A short synthesis of biologically active lignan analogues (pg 331, 2001)
Authors: Kamlage, S Sefkow, M Zobel, BL Peter, MG
Citation: S. Kamlage et al., A short synthesis of biologically active lignan analogues (pg 331, 2001), CHEM COMMUN, (5), 2001, pp. 507-507
A short synthesis of biologically active lignan analogues
Authors: Kamlage, S Sefkow, M Pool-Zobel, BL Peter, MG
Citation: S. Kamlage et al., A short synthesis of biologically active lignan analogues, CHEM COMMUN, (4), 2001, pp. 331-332
Synthesis of (+)-wikstromol by double alkylation of malic acid
Authors: Sefkow, M
Citation: M. Sefkow, Synthesis of (+)-wikstromol by double alkylation of malic acid, TETRAHEDR-A, 12(7), 2001, pp. 987-989
Enantioselective synthesis of alpha-hydroxylated enterolactone and analogs
Authors: Sefkow, M Kelling, A Schilde, U
Citation: M. Sefkow et al., Enantioselective synthesis of alpha-hydroxylated enterolactone and analogs, TETRAHEDR L, 42(30), 2001, pp. 5101-5104
Enantioselective synthesis of (-)-wikstromol using a new approach via malic acid
Authors: Sefkow, M
Citation: M. Sefkow, Enantioselective synthesis of (-)-wikstromol using a new approach via malic acid, J ORG CHEM, 66(7), 2001, pp. 2343-2349
Crystal structure of (3aR,4 ' R,7R,7aS)-tetrahydro-7-hydroxy-2,2,2 ' 2 '-tetramethylspiro[1,3-benzodioxole-5 (4H),4 '-[1,3]dioxolan]-5 '-one, C13H20O6
Authors: Kelling, A Schilde, U Sefkow, M
Citation: A. Kelling et al., Crystal structure of (3aR,4 ' R,7R,7aS)-tetrahydro-7-hydroxy-2,2,2 ' 2 '-tetramethylspiro[1,3-benzodioxole-5 (4H),4 '-[1,3]dioxolan]-5 '-one, C13H20O6, Z KRIST-NEW, 215(4), 2000, pp. 513-514
Crystal structure of (1R,2R,4S,6R,8S)-2 ',2 '-dimethoxy-8-hydroxy-spiro[3,5,10-trioxa-tricyclo[6.2.1.0(2,6)]undecan-4,1 '-cyclohexan]-9-one monohydrate, C15H24O8 and of (1R,2R,4R,6R,8S)-2 ',2 '-dimethoxy-8-hydroxyspiro[3,5,10-trioxatricyclo[6.2.1.0(2'6)]undecan-4,1 '-cyclohexan]-9-one, C15H22O7
Authors: Kelling, A Schilde, U Sefkow, M
Citation: A. Kelling et al., Crystal structure of (1R,2R,4S,6R,8S)-2 ',2 '-dimethoxy-8-hydroxy-spiro[3,5,10-trioxa-tricyclo[6.2.1.0(2,6)]undecan-4,1 '-cyclohexan]-9-one monohydrate, C15H24O8 and of (1R,2R,4R,6R,8S)-2 ',2 '-dimethoxy-8-hydroxyspiro[3,5,10-trioxatricyclo[6.2.1.0(2'6)]undecan-4,1 '-cyclohexan]-9-one, C15H22O7, Z KRIST-NEW, 215(4), 2000, pp. 515-518
Selective protection of either the phenol or the hydroxy group in hydroxyalkyl phenols
Authors: Sefkow, M Kaatz, H
Citation: M. Sefkow et H. Kaatz, Selective protection of either the phenol or the hydroxy group in hydroxyalkyl phenols, TETRAHEDR L, 40(36), 1999, pp. 6561-6562
Epothilone A-D and their thiazole-modified analogs as novel anticancer agents
Authors: Hofle, G Glaser, N Leibold, T Sefkow, M
Citation: G. Hofle et al., Epothilone A-D and their thiazole-modified analogs as novel anticancer agents, PUR A CHEM, 71(11), 1999, pp. 2019-2024
Stereoselective cross-coupling of benzylic bromides and vinyl stannanes
Authors: Kamlage, S Sefkow, M Peter, MG
Citation: S. Kamlage et al., Stereoselective cross-coupling of benzylic bromides and vinyl stannanes, J ORG CHEM, 64(8), 1999, pp. 2938-2940
Substitutions at the thiazole moiety of epothilone
Authors: Sefkow, M Hofle, G
Citation: M. Sefkow et G. Hofle, Substitutions at the thiazole moiety of epothilone, HETEROCYCLE, 48(12), 1998, pp. 2485-2488
Risultati: 1-14 |