100
Views
2
CrossRef citations to date
0
Altmetric
Original Articles

Stereoselective Synthesis Of Homo-Apioneplanocin A As Potential Inhibitor Of S-Adenosylhomocysteine Hydrolase

, , , , , , & show all
Pages 729-732 | Published online: 10 Dec 2007

REFERENCES

  • Yaginuma , S. , Muto , N. , Tsujino , M. , Sudate , Y. , Hayashi , M. and Otani , M. 1981 . Studies on neplanocin A, new antitumor antibiotic. I. Producing organism, isolation and characterization . J. Antibiot. , 34 : 359 – 366 .
  • Kishi , T. , Muroi , M. , Kusaka , T. , Nishikawa , M. , Kamiya , K. and Mizuno , K. 1972 . Chem. Pharm. Bull. , 20 : 940
  • Borchardt , R. T. , Keller , B. T. , Patel-Thombre , U. and Neplanocin , A. 1984 . A potent Inhibitor of S-adenosylhomocysteine hydrolase and of vaccinia virus multiplication in mouse L929 cells . J. Biol. Chem. , 259 : 4353 – 4358 .
  • Shuto , S. , Obara , T. , Toriya , M. , Hosoya , M. , Snoeck , R. , Andrei , G. , Balzarini , J. and De Clercq , E. 1992 . New Neplanocin Analogs. 1. Synthesis of 6′-modified neplanocin A derivatives as broad-spectrum antiviral agents . J. Med. Chem. , 35 : 324 – 331 .
  • Terao , Y. , Akamatsu , M. and Achiwa , K. 1991 . Synthesis of chiral 3-substituted gamma-lactones and 9-furanosyladenine from (R)-2-(2,2-diethoxyethyl)-1,3-propanediol monoacetate prepared by lipase-catalyzed reaction . Chem. Pharm. Bull. , 39 : 823 – 825 .
  • Moon , H. R. , Kim , H. O. , Lee , K. M. , Chun , M. W. , Kim , J. H. and Jeong , L. S. 2002 . Stereoselective synthesis of a novel apio analogue of neplanocin A as potential S-adenosylhomocysteine hydrolase iinhibitor . Org. Lett. , 4 : 3501 – 3503 .
  • Shuto , S. , Obara , T. , Saito , Y. , Andrei , G. , Snoeck , R. , De Clercq , E. and Matsuda , A. 1996 . New neplanocin analogues. 6. Synthesis and potent antiviral acitivity of 6′-homoneplanocin A . J. Med. Chem. , 39 : 2392 – 2399 .
  • Naka , T. , Minakawa , N. , Abe , H. , Kaga , D. and Matsuda , A. 2000 . The stereoselective synthesis of 4′-β-thioribonucleosides via the Pummerer reaction . J. Am. Chem. Soc. , 122 : 7233 – 7243 .

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.