as illustrated by the rales of consumption of the active hydrogen atoms of BTA via the competitive Michael addition reaction
(corresponding to the term [K.sub.M] [B.sub.H] [M] in Eq.
General Procedure for the Michael Addition Reaction
of Indole with [beta]-Nitroolefins Catalyzed by Feist's Acid (GP1).
Therefore, we showed the diastereoselective synthesis of S,S-2-methylsulfanyl-2-methylsulfinyl-1indanol (7) by reduction reaction using 2-methylsulfanyl-2-methylsulfinyl-1-indanone (9) optically enriched demonstrating the high efficiency of the sulfoxide group on the control of asymmetric induction in the carbonyl addition reaction
When the reaction was performed using higher concentration solution (0.5 M) for the reaction mixture, only the isomerized trans product was formed in trace amounts with no addition reaction
taking place in all three methods.
The Type I coagent is a very reactive monomer, favoring addition reactions
leading to homopolymerization and subsequent grafting to polymer chains, through either direct addition reactions
(unsaturated polymers) or through abstraction/coupling reactions with saturated or unsaturated polymer chains.
(9.) Mather, BD, Viswanathan, K, Miller, KM, Long, TE, "Michael Addition Reactions
in Macromolecular Design for Emerging Technologies." Prog.
with formation of carbon-oxygen bonds: (iii) Glycol forming reactions.
 "Related Pergamon Titles of Interest," in Conjugate Addition Reactions
in Organic Synthesis, vol.
The extent of both combination and addition reactions
will depend on the peroxide level, whereas only the extent of the addition reaction
is affected by the diene type and content.
Isomerization versus Addition reactions
of Maleic Acid and its Methyl Ester-A systematic study on the effect of Temperature, Concentration and Reagents/Catalysts Nagarajan Vasumathi, Ashley Casey and Jill Lott, Dept.
A high ROOH concentration therefore implies a high concentration of conjugated double bonds that are especially prone to radical addition reactions
, because of the possibility of forming a relatively stable allylic radical.
His textbook looks at acid, bases, and nucleophiles; and substitution, elimination, and addition reactions
. He includes answers and explanations for the chapter-end problems.