FACILE RADICAL DECARBOXYLATIVE ALKYLATION OF HETEROAROMATIC BASES USING CARBOXYLIC ACIDS AND TRIVALENT IODINE COMPOUNDS

DOI: 10.1016/0040-4039(91)80221-Q

Source and publish data:

Tetrahedron Letters p. 6559 - 6562 (1991)

Update date:2022-08-04

Topics:

Authors:

Togo, Hideo

Aoki, Masahiko

Yokoyama, Masataka

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

Article abstract of DOI:10.1016/0040-4039(91)80221-Q

Many kinds of heteroaromatic bases were easily alkylated by the reaction of carboxylic acids with benzene or pentafluorobenzene via radical decarboxylative pathways.This system was further applied to the reaction with tetrahydrofurylcarboxylic acid, 1-(2,3,5-tri-O-benzyl)-D-ribofuranosylacetic acid, and 1-(2,3,5-tri-O-benzyl)-D-ribofuranosylcarboxylic acid for the model synthesis of C-nucleosides.

Full text of DOI:10.1016/0040-4039(91)80221-Q

Products guided by the article

Product name:1-Propanone, 1-(4-methyl-2-quinolinyl)-3-phenyl-

Cas No:138715-87-4

R&D Labs maybe for 138715-87-4

Jiaxing Trustworthy Import And Export Co.,Ltd

Contact:+86-573-82030555

Address:Room 1202, Unit B, Charming plaza,No.1558 East Zhongshan Road , Jiaxing City, Zhejiang Province, China.
taizhou creating bio-pharm co.,ltd.

Contact:+86- 576- 88827176

Address:715 room ,unit A.junyue Building,Jiaojiang,Taizhou,Zhejiang,China
Liaoning Yufeng Chemical Co.,Ltd.

Contact:86-0419-3418888

Address:The metallurgical industrial zone,shoushan town, Liaoyang, Liaoning, China
Binzhou Holly Pharmaceutical Co.,Ltd.

Contact:74517

Address:No.15 Dapu Road,Huangpu District Shanghai,P.R.China
Wuhan Jadechem International Trade Co.,Ltd.

website:http://www.jadechem-intl.com

Contact:+86-27-83527060

Address:Room 502,Building C11,Software new city No.8,Huacheng Avenue,East Lake High-tech development zone,Wuhan,Hubei,China

Relevant to this article

Ethene complexes of bulky titanocenes, their thermolysis, and their reactivity toward 2-butyne

Doi:10.1021/om300461k
(2012)
Synthesis of desacetamido P-3A: 1,3,5-triazine → pyrimidine heteroaromatic azadiene Diels-Alder reaction

Doi:10.1021/jo00032a001
(1992)
Design, synthesis characterization and in vitro biological activity of a series of 3-aryl-6-(bromoarylmethyl)-7H-thiazolo[3,2-b]-1, 2, 4-triazin-7-one derivatives as the novel acetylcholinesterase inhibitors

Doi:10.1016/j.cclet.2012.04.022
(2012)
Design, synthesis and spectroscopic and crystallographic characterisation of novel functionalized pyrazole derivatives: biological evaluation for their cytotoxic, angiogenic and antioxidant activities

Doi:10.1007/s11164-018-3445-6
(2018)
A Facile Ring Transformation of 5-Aminopyrimidin-4(3H)-one into 2-Alkoxy-1H-imidazoles in the Presence of Oxidative Metal Salts and Alkyl Alcohols

Doi:10.1039/c39910001688
(1991)
Syntheses of proline analogues as potential mechanism-based inhibitors of proline dehydrogenase: 4-methylene-L-, (E)- and (Z)-4-(fluoromethylene)-L-, cis- and trans-5-ethynyl-(±)-, and cis- and trans-5-vinyl-L-proline

Doi:10.1021/jo00033a029
(1992)

Hot Product

9012-76-4
629-59-4
20554-84-1
83048-65-1
2687-91-4 N-Ethyl Pyrrolidone good supplier in Chi
84650-60-2
16941-32-5
122-99-6
57-13-6
202138-50-9
57866-21-4
135-19-3
864070-44-0
372-75-8
1484-13-5
103-81-1
7647-15-6
9050-36-6
71-30-7
4584-49-0
75-75-2
135236-72-5
53338-20-8
2687-91-4
61-82-5
51-35-4
590-46-5
110-13-4
5949-29-1
503612-47-3
55289-06-0
497-30-3

Article Doi