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Chemistry Forums for Students => Organic Chemistry Forum => Topic started by: java on January 04, 2007, 05:09:47 PM

Title: bismethylation
Post by: java on January 04, 2007, 05:09:47 PM
Very odd ..i posted this and it didn't show ...oh well I'll try again..

I recently was studying a reaction when the term  "bismethylation" came on and wanting to know what they ment, the authors, I looked it up in goolge and no direct answer ...something about the adjacent carbon to the carbonyl ..? maybe dual methylation is occuring ...I have no clue aside that the article is about methylation ...any information?...java
Title: Re: bismethylation
Post by: chiralic on January 04, 2007, 05:47:01 PM
Hello my "virtual friend" Java:

I saw a abstract on Australian Journal of Chemistry,  where the bismethylation reaction is used to prepare imide, which can be converted into the cis-diester...

Check this link: http://www.publish.csiro.au/nid/51/paper/CH9901941.htm (I don't have access to this journal)

Espero que hayas pasado unas felices fiestas de navidad y año nuevo en union de los tuyos!!!

Regards

Chiralic

Title: Re: bismethylation
Post by: java on January 05, 2007, 06:39:43 AM
Quote
Multiplying prefixes are used in much the same way to denote other identical structural features of a chemical compound, such as principal characteristic groups, sites of unsaturation, and number of ionic centers. However, the multiplying prefixes "bis-", "tris-", etc., are used instead of "di-", "tri-", etc., when the use of the latter would result in a potential ambiguity; for example, tris(decyl) is used to describe three decyl substituents because tridecyl is the name for a thirteen carbon acyclic substituent

..source.

http://www.chem.qmul.ac.uk/iupac/misc/numb.html


So in the defination of bismethylation , it simply means two methylations....java