Synthesis of amino-1,4-anhydro-d-pentitols and amino-1,5-anhydro-d-hexitols with the arabino configuration from (R)-glycidol
暂无分享,去创建一个
S. Castillón | Y. Díaz | F. Bravo | M. Matheu | S. Aragonès
[1] S. Castillón,et al. An expeditious and efficient procedure for the synthesis of unsaturated acyclonucleosides of Z configuration related to D4T. , 2003, The Journal of organic chemistry.
[2] J. Caille,et al. Hetero Diels−Alder-Biocatalysis Approach for the Synthesis of (S)-3-[2-{(Methylsulfonyl) oxy}ethoxy]-4-(triphenylmethoxy)-1-butanol Methanesulfonate, a Key Intermediate for the Synthesis of the PKC Inhibitor LY3335311 , 2002 .
[3] S. Castillón,et al. Stereoselective synthesis of both enantiomers of 1,4-anhydro-alditols, 1,4-anhydro-2-amino-alditols and d- and l-isonucleosides from 2,3-O-isopropylidene-d-glyceraldehyde using iodine-induced cyclization as the key step , 2001 .
[4] S. Castillón,et al. Synthesis of Substituted Tetrahydrofuran by Electrophile‐Induced Cyclization of 4‐Pentene‐1,2,3‐triols − An Example of 5‐exo versus 5‐endo Cyclization Governed by the Electrophile , 2001 .
[5] Y. Ru,et al. Cyclic ketone inhibitors of the cysteine protease cathepsin K. , 2001, Journal of medicinal chemistry.
[6] R. Ife,et al. Diastereoselective synthesis, activity and chiral stability of cyclic alkoxyketone inhibitors of cathepsin K. , 2001, Bioorganic & medicinal chemistry letters.
[7] S. Zook,et al. A concise synthesis of the HIV-protease inhibitor nelfinavir via an unusual tetrahydrofuran rearrangement , 2000 .
[8] S. Christie,et al. Homologation of allylic alcohols. An approach to cyclic and acyclic polyoxygenated compounds , 2000 .
[9] V. Nair,et al. Synthesis and antiviral studies of unsaturated analogues of isomeric dideoxynucleosides. , 1999, Nucleosides & nucleotides.
[10] S. Castillón,et al. Synthesis of Purine and Pyrimidine Isodideoxynucleosides from (S)-Glycydol Using Iodoetherification as Key Step. Synthesis of (S,S)-iso-ddA1 , 1999 .
[11] P. Herdewijn,et al. Synthesis and conformational analysis of 1,5-anhydro-2,4-dideoxy-D-mannitol nucleosides , 1999 .
[12] P. O’Brien,et al. Unexpected effect of protecting group and solvent on the stereoselectivity of m-CPBA epoxidation of diprotected cis-4,5-dihydroxycyclohexenes , 1999 .
[13] B. Schmidt. Epoxide opening reactions of aryl substituted dihydropyran oxides: regio- and stereochemical studies directed towards deoxy-aryl-C-glycosides , 1999 .
[14] B. Kim,et al. Synthesis of novel, optically active, heterocyclic amino alcohols through desymmetrization of a C2-symmetric cyclic sulfate , 1998 .
[15] M. Faul,et al. Macrocyclic Bisindolylmaleimides: Synthesis by Inter- and Intramolecular Alkylation , 1998 .
[16] H. Altenbach,et al. Preparation of S-(−)-2-acetoxymethyl-2,5-dihydrofuran and S-(−)-N-Boc-2-hydroxymethyl-2,5-dihydropyrrole by enzymatic resolution , 1998 .
[17] M. Pineschi,et al. Difuntionalised oxirane systems. Stereodivergent synthesis of 1,4;2,3-dianhydro-5-O-benzyl-l-lyxitol and -l-ribitol , 1997 .
[18] R. R. Talekar,et al. Synthesis of some pyrrolo[2,3-d]pyrimidine and 1,2,3-triazole isonucleosides , 1997 .
[19] Cristina Gardelli,et al. Regiochemical control of the ring opening of 1,2-epoxides by means of chelating processes.9. Synthesis and ring opening reactions of cis- and trans-oxides derived from 3-(benzyloxymethyl)cyclopentene and methyl 2-cyclopenten-1-carboxylate 1 , 1995 .
[20] S. Shuto,et al. Nucleosides and nucleotides. 132. Synthesis and biological evaluations of ring-expanded oxetanocin analogues: Purine and pyrimidine analogues of 1,4-anhydro-2-deoxy-d-arabitol and 1,4-anhydro-2-deoxy-3-hydroxymethyl-d-arabitol , 1994 .
[21] J. Falck,et al. Novel conversion of epoxides to one carbon homologated allylic alcohols by dimethylsulfonium methylide , 1994 .
[22] Cristina Gardelli,et al. Regiochemical control of the ring opening of 1,2-epoxides by means of chelating processes. 8. Synthesis and ring opening reactions of cis- and trans- oxides derived from 3-benzyloxycyclohexene and 2-benzyloxy-5,6-dihydro-2H-pyran , 1994 .
[23] T. Sells,et al. Novel isomeric dideoxynucleosides as potential antiviral agents , 1994 .
[24] Cristina Gardelli,et al. REGIOCHEMICAL CONTROL OF THE RING-OPENING OF 1,2-EPOXIDES BY MEANS OF CHELATING PROCESSES .5. SYNTHESIS AND REACTIONS OF SOME 2,3-EPOXY-1-ALKANOL DERIVATIVES , 1993 .
[25] V. Nair,et al. Isodideoxynucleosides : a conceptually new class of nucleoside antiviral agents , 1992 .
[26] P. Crotti,et al. Alternating high regioselection in methyl group transfer to alicyclic oxiranes. Significance of the presence of a remote polar group , 1989 .
[27] P. Carlier,et al. Regioselective azide opening of 2,3-epoxy alcohols by [Ti(O-i-Pr)2(N3)2]: synthesis of .alpha.-amino acids , 1988 .
[28] S. Gero,et al. Ouverture régiospécifique d'un oxirane preparé á partir du d-xylose par des carbanions soufres , 1981 .
[29] J. Montgomery,et al. ISONUCLEOSIDES. 2. PURINE AND PYRIMIDINE DERIVATIVES OF 1,4‐ANHYDRO‐2‐DEOXY‐D‐ARABINITOL , 1978 .
[30] D. D. Perrin,et al. Purification of Laboratory Chemicals , 2022 .
[31] H. Staudinger,et al. Über neue organische Phosphorverbindungen III. Phosphinmethylenderivate und Phosphinimine , 1919 .