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All posts   Subject: Alkynes as precursors: benzannulation   Please login to post  

 
    yinga
(Hive Bee)
02-17-04 03:50
No 489207
      Alkynes as precursors: benzannulation
(Rated as: good read)
    

It would appear that by choosing the appropriate starting materials, one can synthesize many different substituted benzene rings, including substituents like 1,2-methylenedioxy rings.  I uploaded two articles about these types of reactions at http://www.geocities.com/yingabee/.

For example, regarding http://www.geocities.com/yingabee/JOCv68p5961.pdf, one could choose 10 on the bottom of page 5963 with R being an N-protected (so it won't compete for substitution with the -OTs) NH2-CH2 group, and simple acetylene instead of the 2a/2b, to make phenethylamine.  There are gobs more references on these reactions, with ways to regioselectively put a variety substituents on the product benzene ring but obviously I haven't yet researched extensively.

What do ya think?
 
 

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