Synthesis of (+)-l-[(lα,2α,3β,4α)-2,3-Dihydroxy-4-Hydroxymethyl] -5-Methyl-2,4-(1H, 3H) Pyrimidinedione, the Carbocyclic Analogue of Ara-T

Tai-Shun Lin Department of Pharmacology and Comprehensive Cancer Center, Yale University School of Medicine, New Haven, Connecticut, 06510

Xiao-Hui Zhang Department of Pharmacology and Comprehensive Cancer Center, Yale University School of Medicine, New Haven, Connecticut, 06510

Zi-Hou Wang Department of Pharmacology and Comprehensive Cancer Center, Yale University School of Medicine, New Haven, Connecticut, 06510

W. H. Prusoff Department of Pharmacology and Comprehensive Cancer Center, Yale University School of Medicine, New Haven, Connecticut, 06510

Citations (6)

Keep up to date with the latest research on this topic with citation updates for this article.

Read on this site (1)

Tai-Shun Lin, Ji-Yu Guo & Xiao-Hui Zhang. (1990) Synthesis and Anticancer Activity of 3-(3-Oxoprop-1-enyl)-Substituted Analogues of Carbocyclic Pyrimidine Nucleosides and 2′,3′-Dideoxy Pyrimidine Nucleosides. Nucleosides and Nucleotides 9:7, pages 923-935.
Read now

Articles from other publishers (5)

Aya Kato, Yuri Yasuda, Yoshiaki Kitamura, Mahmoud Kandeel & Yukio Kitade. (2012) Carbocyclic thymidine derivatives efficiently inhibit Plasmodium falciparum thymidylate kinase (PfTMK). Parasitology International 61:3, pages 501-503.
Crossref

Nury Pérez & Barbara Gordillo. (2003) Rapid synthesis of (±)-r-7-benzyloxymethyl-cyclopenta-cis-[4,5][1,3]-oxazolo[3,2-a]pyrimidinones versatile carbocyclic nucleoside precursors. Tetrahedron 59:5, pages 671-676.
Crossref

L. A. Agrofoglio & S. R. ChallandL. A. Agrofoglio & S. R. Challand. 1998. Acyclic, Carbocyclic and L-Nucleosides. Acyclic, Carbocyclic and L-Nucleosides 174 255 .

Luigi Agrofoglio, Edouard Suhas, Audrey Farese, Roger Condom, S. Richard Challand, Robert A. Earl & Roger Guedj. (1994) Synthesis of carbocyclic nucleosides. Tetrahedron 50:36, pages 10611-10670.
Crossref

T.-S. LIN, X.-H. ZHANG, Z.-H. WANG & W. H. PRUSOFF. (1988) ChemInform Abstract: Synthesis of (.+-.)-1-((1α,2α,3β,4α)-2,3-Dihydroxy-4-hydroxymethylcyc# lopentyl)-5-methyl-2,4-(1H,3H)-pyrimidinedione, the Carbocyclic Analogue of Ara-T.. ChemInform 19:48.
Crossref

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:

Order Reprints Request Corporate Permissions

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:

Request Academic Permissions

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.

Synthesis of (+)-l-[(lα,2α,3β,4α)-2,3-Dihydroxy-4-Hydroxymethyl] -5-Methyl-2,4-(1H, 3H) Pyrimidinedione, the Carbocyclic Analogue of Ara-T

Articles from other publishers (5)

Information for

Open access

Opportunities

Help and information

Your download is now in progress and you may close this window

Login or register to access this feature

Synthesis of (+)-l-[(lα,2α,3β,4α)-2,3-Dihydroxy-4-Hydroxymethyl] -5-Methyl-2,4-(1H, 3H) Pyrimidinedione, the Carbocyclic Analogue of Ara-T

Citations (6)

Read on this site (1)

Articles from other publishers (5)

Reprints and Corporate Permissions

Academic Permissions

Related research

To cite this article:

Download citation

Information for

Open access

Opportunities

Help and information

Keep up to date