General Procedure for the Michael
Addition Reaction of Indole with Pyrrole Catalyzed by Feist's Acid (G[P.sub.2]).
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 [Br.sub.2] as a catalyst without adding any bromoform, only isomerized product was formed with no
addition reaction taking place in all three methods.
The Michael
addition reaction between AP (37.5 g; 0.5 mole) and DEM (86.1 g; 0.5 mole) was performed by adding the maleate dropwise under a nitrogen environment to the aminoalcohol at 60[degrees]C over 7 h.
After screening many temperature systems, we pursued the
addition reaction of oleic acid by the [1, 3, 4] thiadiazde derivatives at temperature systems in detail.
Nevertheless, the potential Michael
addition reactions cannot be ruled out because each BTA molecule contains two >NH groups and one >[CH.sub.2] group and the active hydrogen atoms of these functional groups may lake part in the polymerization of BMI with BTA via the Michael
addition reaction mechanism.
Melamine is a good nucleophile; the
addition reaction with the electrophilic formaldehyde occurs under most pH conditions, although the reaction rate is slower at neutral pH.
Moreover, Compound 135 reacted easily with urea in AcOH to afford 2,4-diaminopyrimidobenzothiazepine 147 (65% yield) via cyclo-condensation
addition reaction.
In the second step, the enamine A attack to aromatic aldehydes (
addition reaction) to give intermediates B, which further undergoes dehydration reaction to give 1,6-naphthyridine 3 (Step 3).
Hydrosilylation, which is the
addition reaction of a hydride terminated silane compound to a multiple bond [4], has been recently investigated as a possible method for polymer functionalization in solution [5].
Caption: FIGURE 4: Energy profiles for competitive channels of oxidative
addition reaction.