Carbocyclic Analogues of 5'-Amino-5'-deoxy- and 3'-Amino-3'-deoxythymidines

DOI: 10.1021/jm00154a010

Source and publish data:

Journal of Medicinal Chemistry p. 483 - 488 (1986)

Update date:2022-08-17

Topics:

Authors:

Shealy, Y. Fulmer

O'Dell, C. Allen

Shannon, William M.

Arnett, Gussie

Read Full Text PDF DownLoad Join now for total 90,000,000 free articles

Article abstract of DOI:10.1021/jm00154a010

The carbocyclic analogue of 5'-amino-5'-deoxythymidine was synthesized from the carbocyclic analogue of 2,5'-O-anhydrothymidine acetate.The carbocyclic analogues of 3'-amino-3'-deoxythymidine and of 1-(3'-amino-2',3'-dideoxylyxofuranosyl)thymidine (an all

Full text of DOI:10.1021/jm00154a010

Products guided by the article

Product name:C-5'-O-trityl-2,3'-anhydrothymidine

Cas No:87470-97-1

R&D Labs maybe for 87470-97-1

Beijing Stable Chemcial Co.ltd

Contact:86-10-63785052

Address:A1301 Technological Edifice. No.4 FuFeng Road,FengTai District, Beijing. China
Xuzhou Tianrun Chemical Co.,Ltd

website:http://www.tianrunchem.cn

Contact:86-516-83832636

Address:fuxing road
Zha Yan

Contact:+86-13914766747

Address:Floors 21&22, Jin Cheng Tower, No. 216 Middle Longpan Road, Nanjing
Xian Changyue Biological Technology Co., Ltd.

website:https://www.xachangyue.com/

Contact:+86-029-62886900

Address:Keji Road NO.70
Shanghai Massive Chemical Technology Co., Ltd.

website:http://www.massivechem.com/

Contact:+86 21 34943721

Address:Room 435, 4th floor, Building 9, No. 2568 Gudai Road,Minhang District, Shanghai,

Relevant to this article

A stereoselective access to functional dienes containing a trifluoromethyl group via stille cross coupling of ethyl 4,4,4-trifluoro-3-iodobutenoate

Doi:10.1055/s-1998-1787
(1998)
C-H and N-H Bond Annulation of Benzamides with Isonitriles Catalyzed by Cobalt(III)

Doi:10.1055/s-0036-1589011
(2017)
Formation of HCOH + H2 through the Reaction CH3 + OH. Experimental Evidence for a Hitherto Undetected Product Channel

Doi:10.1002/kin.550270608
(1995)
Catalytic and Mechanistic Developments of the Nickel(II) Pincer Complex-Catalyzed Hydroarsination Reaction

Doi:10.1002/chem.201902138
(2019)
Doi:10.1007/s12122-002-1031-5
()
Doi:10.1021/jo00982a012
(1972)

Article Doi