Enantiomeric synthesis of nucleosides

[1]  C. Hourioux,et al.  Stereoselective synthesis of α-l-bicarbocyclic nucleosides as potential antiviral drugs , 1998 .

[2]  L. Agrofoglio,et al.  A SHORT AND STEREOSELECTIVE SYNTHESIS OF CARBOCYCLIC ALPHA-L-DIDEOXYHOMONUCLEOSIDES , 1998 .

[3]  C. K. Chu,et al.  Asymmetric synthesis of L-cyclopentyl carbocyclic nucleosides , 1997 .

[4]  E. Garvey,et al.  Unique intracellular activation of the potent anti-human immunodeficiency virus agent 1592U89 , 1997, Antimicrobial agents and chemotherapy.

[5]  V. Marquez,et al.  Conformationally locked carbocyclic nucleosides built on abicyclo[3.1.0]hexane template with a fixed Southern conformation.Synthesis and antiviral activity , 1997 .

[6]  R. Wagner,et al.  Nucleosides with a twist. Can fixed forms of sugar ring pucker influence biological activity in nucleosides and oligonucleotides , 1996 .

[7]  Y. Cheng,et al.  Use of 2'-fluoro-5-methyl-beta-L-arabinofuranosyluracil as a novel antiviral agent for hepatitis B virus and Epstein-Barr virus , 1995, Antimicrobial agents and chemotherapy.

[8]  L. Agrofoglio,et al.  Synthesis of carbocyclic nucleosides , 1995 .

[9]  J. Wakefield,et al.  Inhibition of human immunodeficiency virus type 1 reverse transcriptase by the 5'-triphosphate beta enantiomers of cytidine analogs , 1994, Antimicrobial Agents and Chemotherapy.

[10]  H. Mitsuya,et al.  Conformationally locked nucleoside analogues. Synthesis of dideoxycarbocyclic nucleoside analogues structurally related to neplanocin C. , 1994, Journal of medicinal chemistry.

[11]  K. Eger,et al.  Synthesis of new acyclic pyrimidine nucleoside analogs as potential antiviral drugs. , 1994, Journal of medicinal chemistry.

[12]  Y. Cheng,et al.  Synthesis and biological evaluation of 2',3'-dideoxy-L-pyrimidine nucleosides as potential antiviral agents against human immunodeficiency virus (HIV) and hepatitis B virus (HBV). , 1994, Journal of medicinal chemistry.

[13]  A. D. Borthwick,et al.  Synthesis of Chiral Carbocyclic Nucleosides , 1992 .

[14]  R. Schinazi,et al.  Activities of the four optical isomers of 2',3'-dideoxy-3'-thiacytidine (BCH-189) against human immunodeficiency virus type 1 in human lymphocytes , 1992, Antimicrobial Agents and Chemotherapy.

[15]  M. Okabe,et al.  A cyclopropano analog of 2',3'-dideoxycytidine: stereoselective formation of a [3,1,0] bicyclic system via homologous ferrier reaction , 1989 .

[16]  S. Larson,et al.  Synthesis, intramolecular hydrogen bonding, and biochemical studies of clitocine, a naturally occurring exocyclic amino nucleoside. , 1988, Journal of medicinal chemistry.

[17]  Mujo Kim,et al.  Synthesis of clitocine, a new insecticidal nucleoside from the mushroom Clitocybe inversa , 1988 .

[18]  H. Naoki,et al.  Clitocine, a new insecticidal nucleoside from the mushroom clitocybe inversa , 1986 .

[19]  J. Jiricny,et al.  The benzoylation of uracil and thymine , 1984 .

[20]  P. M. Lesko,et al.  Intramolecular .alpha.-amidoalkylation of an olefin for the synthesis of a useful prostaglandin intermediate , 1981 .

[21]  O. Mitsunobu The Use of Diethyl Azodicarboxylate and Triphenylphosphine in Synthesis and Transformation of Natural Products , 1981 .

[22]  H. Schaeffer,et al.  Pyrimidine acyclic nucleosides. 5-Substituted 1-[(2-aminoethoxy)methyl]uracils as candidate antivirals. , 1981, Journal of medicinal chemistry.

[23]  M. Uskoković,et al.  Asymmetric synthesis of prostaglandin intermediates. , 1973, Journal of the American Chemical Society.

[24]  Y. Shealy,et al.  Synthesis of carbocyclic analogs of purine ribonucleosides , 1969 .

[25]  N. Kawabata,et al.  Synthesis of cyclopropanes by the reaction of olefins with dialkylzinc and methylene iodide , 1968 .

[26]  Y. Shealy,et al.  9-[β-DL-2α,3α-Dihydroxy-4β-(hydroxymethyl)- cyclopentyl]adenine, the Carbocyclic Analog of Adenosine1,2 , 1966 .

[27]  H. Simmons,et al.  A New Synthesis of Cyclopropanes1 , 1959 .