Stereoselective synthesis of 3'-deoxy-3'-fluoroadenosine

DOI: 10.1246/bcsj.62.2119

Source and publish data:

Bulletin of the Chemical Society of Japan p. 2119 - 2120 (1989)

Update date:2022-07-29

Topics:

Authors:

Morizawa

Nakayama

Yasuda Yasuda

Uchida Uchida

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

Article abstract of DOI:10.1246/bcsj.62.2119

Full text of DOI:10.1246/bcsj.62.2119

Products guided by the article

Product name:methyl 2-O-benzyl-5-O-t-butyldimethylsilyl-β-D-xylofuranoside

Cas No:112668-55-0

R&D Labs maybe for 112668-55-0

KA-SHING Business Trade Macau Co., Ltd.

Contact:00853-28430045

Address:23rd Floor, Block 3 La Cite, Areia Preta, Macao
HOST COUNTRY LIMITED

Contact:+852 83038667

Address:Room 1502, 15th Floor, SPA Centre,53-55 Lockhart Road, Wanchai, Hong Kong
FREEBARQUE DEVELOPMENT GROUP LIMITED

Contact:+86(0)10-5109 5335 or 5109 5345

Address:Room602,Block1-B,LINGDI OFFICE,NO.13 BEIYUAN ROAD
Zhejiang Linhai Xinhua Chemicals Factory

Contact:0086-13661858911

Address:Xunqiao Development Zone, Linhai, Zhejiang, China
Buffett (China) Holding Co.,Ltd

Contact:4006570891

Address:

Relevant to this article

Direct asymmetric Michael addition of thioether-based aryl sulfanyl-propan-2-one to nitroalkenes catalyzed by a chiral amine-thiourea bifunctional organocatalyst

Doi:10.1002/chir.20689
(2010)
Efficient synthesis of novel 2,4-[diaryl-3-azabicyclo[3.3.1]nonan-9-yl]-5- spiro-4-acetyl-2-(acetylamino)-δ²-1,3,4-thiadiazolines

Doi:10.1080/00397910903161694
(2010)
DNA binding and cleavage studies of copper(II) complexes with 2′-deoxyadenosine modified histidine moiety

Doi:10.1007/s00775-015-1282-2
(2015)
Ligand-Tuned C–H Bond Activation/Arylation of 2-Arylpyridines over Pyridine-Based N,O/N,N Ligated Ruthenium–Arene Complexes

Doi:10.1002/ejic.201701446
(2018)
Dramatic Effect of γ-Heteroatom Dienolate Substituents on Counterion Assisted Asymmetric Anionic Amino-Cope Reaction Cascades

Doi:10.1021/jacs.1c00745
(2021)
Phosphoramidate ProTides of 2′-C-methylguanosine as highly potent inhibitors of hepatitis C virus. Study of their in vitro and in vivo properties

Doi:10.1021/jm1003792
(2010)

Article Doi