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14: Reactions with stabilized carbanion intermediates, part II

These pages are under construction.  A complete 2016 edition of Organic Chemistry With a Biological Emphasis is available here as a free PDF download.


We saw in Chapter 13 how stabilized carbanions - enols, enolated enamines - are key intermediates in biological isomerization reactions and in carbon-carbon bond-forming and bond-breaking events.  In this chapter, we will look at two more important reaction types, called Michael additions and β-eliminations, which involve stabilized carbanion species as intermediates. In a Michael addition, a nucleophile and a proton are 'added' to the two carbons of an alkene that is conjugated to a carbonyl. In a beta-elimination, the reverse process occurs:




The rich and fascinating chemistry of coenzymes plays a large role in this chapter.  We will examine several carbanion-intermediate reactions that involve the participation of pyridoxal phosphate (vitamin B6), a very important carbanion-stabilizing coenzyme. Finally, we will see how the coenzyme thiamine (vitamin B1) allows a carbonyl carbon to act as the nucleophile in a unique class of carbon-carbon bond-forming reaction.