Purines. xxxviii. A general synthesis of 7,9-dialkyladeninium salts from 9-alkyladenines by regioselective alkylation: Utilization of an N6-alkoxy group as a control synthon

DOI: 10.1248/cpb.38.652

Source and publish data:

Chemical and Pharmaceutical Bulletin p. 652 - 660 (1990)

Update date:2022-08-03

Topics:

Authors:

Fujii Fujii

Saito Saito

Sakuma Sakuma

Minami Minami

Inoue Inoue

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

Article abstract of DOI:10.1248/cpb.38.652

A detailed account is given of the general synthetic route to 7,9-dialkyladeninium salts (16 18) from N⁶-alkoxy-9-alkyladenines (type 5 or 11--13), readily obtainable from 9-alkyladenines in three steps involving N(1)-oxidation, O-alkylation, a

Full text of DOI:10.1248/cpb.38.652

NII-Electronic Library Service

Products guided by the article

Product name:N⁶-benzyloxy-N⁶-ethyl-9-methyladenine hydrochloride

Cas No:78030-72-5

R&D Labs maybe for 78030-72-5

Xi'an Kaixiang Photoelectric Technology Co., Ltd

website:http://www.kxmaterials.com/

Contact:86-29-15991651477

Address:Building 6, Biopharmaceutical Industry R&D Cluster Base, No. 16, Caotang 4th Road, Caotang Science and Technology Industrial Base, High-tech Zone, Xi'an City, Shaanxi Province, China
Tianjin Hedong Red Cliff Chemical Reagent Factory

Contact:+86-022-84780548

Address:Li Ming Zhuang Gong Ye Yuan,Dongli District,Tianjin,China
Compro Shijiazhuang Fine Chemical Co., Ltd

Contact:0086-311-89689838

Address:Economic and Technological Development Zone of Shijiazhuang,Hebei
Xiamen Goodhealth Pharmchem Co., Ltd.

Contact:0086-592-2097683

Address:404R No.2 54# Minzu Rd., Xiamen, China
Shijiazhuang Haotian Chemical Co., Ltd.

Contact:86-311-85044374

Address:293 Donggang Road

Relevant to this article

A Convenient Way to Novel Fe^IV Complexes with Mixed N/S/P Coordination Spheres and Innocent Ligands

Doi:10.1002/anie.199712011
(1997)
Synthesis of Conjugates of Lupane-Type Pentacyclic Triterpenoids with 2-Aminoethane- and N-Methyl-2-Aminoethanesulfonic Acids. Assessment of in vitro Toxicity

Doi:10.1007/s10600-017-2153-6
(2017)
Enantioselective construction of cyclic ethers by an aldol-cyclization sequence

Doi:10.1021/jo961904z
(1997)
Novel Coupling Reactions of Dithioacetals with Organocuprate Reagents. Propargylic Dithioacetal as an Allene-1,3-Zwitterion Synthon

Doi:10.1021/jo970700v
(1997)
Synthesis of (R)-(2,3,4,5,6-pentadeuterophenyl)oxirane

Doi:10.1002/(SICI)1099-1344(199706)39:6<479::AID-JLCR993>3.0.CO;2-6
(1997)
Active site design in a chemzyme: Development of a highly asymmetric and remarkably temperature-independent catalyst for the imino aldol reaction

Doi:10.1002/1521-3773(20010618)40:12<2271::AID-ANIE2271>3.0.CO;2-N
(2001)

Article Doi