Iodination of aromatic compounds under mild and solvent-free conditions

DOI: 10.1080/00304940209355787

Source and publish data:

Organic Preparations and Procedures International p. 647 - 651 (2002)

Update date:2022-08-11

Topics:

Authors:

Hajipour, Abdol R.

Ruoho, Arnold E.

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Article abstract of DOI:10.1080/00304940209355787

Full text of DOI:10.1080/00304940209355787

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Article Doi

Iodination of aromatic compounds under mild and solvent-free conditions

DOI: 10.1080/00304940209355787

Source and publish data:

Authors:

Article abstract of DOI:10.1080/00304940209355787

Full text of DOI:10.1080/00304940209355787

Products guided by the article

R&D Labs maybe for 135050-44-1

Relevant to this article

Iridium-Catalyzed Enantioselective Allylic Substitution of Enol Silanes from Vinylogous Esters and Amides

A novel photorearrangement of aryl naphthylmethyl ethers. Formation of cyclohexa-2,4-dienone derivatives

Mild and efficient prepare disperse yellow 184, disperse yellow 232 and their analogues via LTTM promoted three-component reaction

Extend Hypervalent 5c-6e Interactions: Linear Alignment of Five C-Se- - -O- - -Se-C Atoms in Anthraquinone and 9-Methoxyanthracene Bearing Arylselanyl Groups at the 1,8-Positions

Transition metal-catalyzed [4 + 2 + 2] cycloadditions of bicyclo[2.2.1]hepta-2,5-dienes (Norbornadienes) and bicyclo[2.2.2]octa-2,5-dienes

Purification, characterization and N-terminal sequence analysis of betel leaf (Piper betle) invertase