ENANTIOSELECTIVE SYNTHESES OF (-)-ANISOMYCIN AND ITS PROPIONATE DERIVATIVE(3097-B1)
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[1] G. Lin,et al. A facile synthesis of (2S,3R,4S)-4-amino-5-cyclohexyl-1- morpholino-2,3-pentanediol, the C-terminal compound of renin inhibitor BW-175 , 1995 .
[2] N. Ikota. SYNTHESIS OF (2R,3R,4R,5R)-3,4-DIHYDROXY-2,5-DI-HYDROXYMETHYLPYRROLIDINE AND (-)-ANISOMYCIN DERIVATIVE FROM (S)-PYROGLUTAMIC ACID DERIVATIVE , 1995 .
[3] 史志才,et al. A synthesis of the polyhydroxylated pyrrolidines: Synthesis of 1,4-dideoxy1,4-dideoxy-1,4-Imino-D-lyxitol andN-benzyl-4- epi-(-)-anisomycin , 1995 .
[4] G. Righi,et al. Regio- and Chemoselective Synthesis of Halohydrins by Cleavage of Oxiranes with Metal Halides , 1994 .
[5] K. B. Sharpless,et al. Asymmetric dihydroxylation of tertiary allylic alcohols , 1993 .
[6] P. Walsh,et al. Modified cinchona alkaloid ligands: Improved selectivities in the osmium tetroxide catalyzed asymmetric dihydroxylation (AD) of terminal olefins , 1993 .
[7] H. Naganawa,et al. Anisomycin and new congeners active against human tumor cell lines. , 1993, Journal of antibiotics (Tokyo. 1968).
[8] H. Kolb,et al. Improved enantioselectivity in asymmetric dihydroxylations of terminal olefins using pyrimidine ligands , 1993 .
[9] Toshizumi Miyamoto,et al. New total synthesis of (+)-N-methylanisomycin by anodic cyclization of δ-alkenylamine , 1993 .
[10] B. Lohray. Recent advances in the asymmetric dihydroxylation of alkenes , 1992 .
[11] P. Andersson,et al. Catalytic asymmetric dihydroxylation of tetrasubstituted olefins , 1992 .
[12] R. Ballini,et al. A nitrone-based approach to the enantioselective total synthesis of (-)-anisomycin , 1992 .
[13] Robert C. Anderson,et al. A highly regioselective conversion of epoxides to halohydrins by lithium halides , 1991 .
[14] May Tajima,et al. Asymmetric intramolecular amidation of N-(tert-butoxycarbonyl)-3-hydroxy-4-pentenylamine. A new entry to chiral building blocks for the synthesis of biologically active nitrogen-containing compounds , 1991 .
[15] T. Gracza,et al. Controlled Synthesis of Enantio-, Regio-, and Diastereomers of Amino-4-pentenediols from 1,4-Pentadien-3-ol via Epoxy-4-pentenols I. erythro-1-Amino-4-pentene-2,3-diols , 1991 .
[16] V. Jäger,et al. Controlled Synthesis of Regio-, Enantio-, and Diastereomers of Amino-4-pentenediols from 1,4-Pentadien-3-ol via Epoxy-4-pentenols II. erythro- and threo-3-Amino-4-pentene-1,2-diols and erythro-2-Benzylamino-4-pentene-1,3-diol , 1991 .
[17] B. Koppenhoefer,et al. Asymmetric sharpless epoxidation of divinylcarbinol. Erythro-D- and -L-4-pentenitols by hydrolysis of regioisomeric epoxy-4-pentenols☆☆☆ , 1991 .
[18] V. Jäger,et al. Cyclization of N‐Protected l‐Amino‐4‐pentene‐2,3‐diols to lxyo‐Configurated Deoxyimino Sugars (cis‐Dihydroxypyrrolidines); Synthesis of Potential Glycosidase Inhibitors , 1990 .
[19] T. Gracza,et al. Regiocontrol in the synthesis of optically active amino-4-pentenediols via epoxy-4-pentenols. Novel acyclic adenosine analogues☆ , 1989 .
[20] M. Zamkanei,et al. Stereospecific synthesis of (-)-anisomycin from D-galactose , 1988 .
[21] S. Jegham,et al. A new synthesis of (−)-anisomycin or (+)-anisomycin starting from D-tyrosine or L-tyrosine , 1988 .
[22] T. Shono,et al. Total synthesis of (−)-anisomycin , 1987 .
[23] Bernhard Koppenhoefer,et al. Quantitative bestimmung der vier konfigurationsisomeren von 4-pententriol durch gaschromatographie an D- und L-chirasil-val , 1987 .
[24] A. Meyers,et al. An asymmetric total synthesis of unnatural (+)-anisomycin , 1987 .
[25] N. Yamazaki,et al. Highly selective total synthesis of enantiomerically pure (−)-anisomycin , 1986 .
[26] V. Jäger,et al. Synthesis of erythro‐D‐ and ‐L‐4‐Pentenetriols. Selective Epoxy Allyl Alcohol Hydrolysis with Retention or Twofold Inversion (Enantiomerization) , 1986 .
[27] H. Paulsen,et al. A new synthesis of (–)-anisomycin and its demethoxy analogue from D-ribose , 1985 .
[28] S. Hatakeyama,et al. Preparation of (2R,3S)-1,2-epoxypent-4-en-3-ol, a new chiral building block for the synthesis of (+)-endo- and (–)-exo-brevicomin , 1985 .
[29] W. Christ,et al. On stereochemistry of osmium tetraoxide oxidation of allylic alcohol systems. Empirical rule , 1983 .
[30] S. Hall,et al. An efficient stereospecific total synthesis of (.+-.)-anisomycin and related new synthetic antibiotics , 1982 .
[31] J. G. Moffatt,et al. Chiral syntheses of the antibiotics anisomycin and pentenomycin from carbohydrates , 1979 .
[32] I. Felner,et al. [Complete synthesis of the antibiotic anisomycin]. , 1970, Helvetica chimica acta.
[33] J. Raa,et al. Total synthesis of anisomycin , 1969 .
[34] E. Oki,et al. Total synthesis of dl-anisomycin. , 1968, Chemical and pharmaceutical bulletin.
[35] J. Raa,et al. Synthesis of optically active deacetyl anisomycin , 1968 .
[36] A. Grollman. Inhibitors of protein biosynthesis. II. Mode of action of anisomycin. , 1967, The Journal of biological chemistry.
[37] F. Tanner,et al. ANISOMYCIN,1 A NEW ANTI-PROTOZOAN ANTIBIOTIC , 1954 .