Facile synthesis of 2'-deoxyisoguanosine and related 2',3'-dideoxyribonucleosides

DOI: 10.1002/hlca.19940770305

Source and publish data:

Helvetica Chimica Acta p. 622 - 630 (1994)

Update date:2022-09-26

Topics:

Authors:

Seela Seela

Gabler Gabler

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

Article abstract of DOI:10.1002/hlca.19940770305

The 2'-deoxyisoguanosine (1) was synthesized by a two-step procedure from 2'-deoxyguanosine (5). Amination of silylated 2'-deoxyguanosine yielded 2-amino-2'-deoxyadenosine (6) which was subjected to selective deamination of the 2-NH₂ group resu

Full text of DOI:10.1002/hlca.19940770305

Products guided by the article

Product name:2-chloro-9-<2-deoxy-5-O-<(1,1-dimethylethyl)diphenylsilyl>-β-D-erythro-pentofuranosyl>-9H-purin-6-amine

Cas No:156834-09-2

R&D Labs maybe for 156834-09-2

Zhonghao (dalian) Research and Design Institute of Chemical Industry Co., Ltd

Contact:+86 411 84674606

Address:201, Huangpu Road , Shahekou District, Dalian ,116023-China
Shanghai Taibao Pharmaceutical Technology Co., Ltd(expird)

Contact:021-52217366

Address:shanghai
SINO Industries Company Limited(expird)

Contact:86-29-85369724

Address:No.111, Jiefang Road, Xi’an, China
Yueyang Hudex Pharmaceuticals Ltd.

Contact:0730-8748800

Address:Wujiang Bridge，Yueyang Economy & Technology Development Zone
Henan Harvest Chem Co., Ltd

Contact:+86-371-86058576

Address:NO.32, Jingsan Road, Zhengzhou, China

Relevant to this article

Propargyl-linked antifolates are dual inhibitors of Candida albicans and Candida glabrata

Doi:10.1021/jm401916j
(2014)
Harnessing by a diacetylene unit: A molecular design for porous two-dimensional network formation at the liquid/solid interface

Doi:10.1039/c3cc47949h
(2014)
B(C6F5)3-Catalyzed Highly Stereoselective Hydrogenation of Unfunctionalized Tetrasubstituted Olefins

Doi:10.1021/acs.orglett.9b02512
(2019)
Substituent effect on the enantioselectivity in lipase-catalyzed transesterification of trans-2,5-disubstituted pyrrolidines

Doi:10.1016/S0040-4020(01)00214-9
(2001)
Synthesis of 6-tetrazolyl-substituted sulfocoumarins acting as highly potent and selective inhibitors of the tumor-associated carbonic anhydrase isoforms IX and XII

Doi:10.1016/j.bmc.2014.01.043
(2014)
Discovery and optimization of a new class of pyruvate kinase inhibitors as potential therapeutics for the treatment of methicillin-resistant Staphylococcus aureus infections

Doi:10.1016/j.bmc.2014.01.020
(2014)

Article Doi