Nucleophilic addition phase-transfer catalysis

Partitioning of carbocations between addition of nucleophiles and deprotonation, 35, 67 Perchloro-organic chemistry structure, spectroscopy and reaction pathways, 25, 267 Permutational isomerization of pentavalent phosphorus compounds, 9, 25 Phase-transfer catalysis by quaternary ammonium salts, 15, 267 Phosphate esters, mechanism and catalysis of nucleophilic substitution in, 25, 99 Phosphorus compounds, pentavalent, turnstile rearrangement and pseudoration in permutational isomerization, 9, 25... 

Typical phase transfer catalysis in liquid-liquid systems combines processes in which Na+ or K+ salts of inorganic and organic anions derived from strong adds (phenolates, thiolates, carboxylates, etc.) are continuously transferred from aqueous (often alkaline) solutions to the organic phase by the phase transfer catalysts. Applications include nucleophilic substitution, addition, elimination, oxidation, and reduction reactions. 

Y. Ali and W. A. Szarek, Synthetic approaches to gem-di-C-alkyl derivatives of carbohydrates Nucleophilic addition reactions of 3-C-methylene compounds derived from l,2 5,6-di-0-isopropylidene-ot-D-rifto-hexofuranos-3-ulose using phase transfer catalysis, Carbohydr. Res. 67 Cll (1978). 

In 1971, Starks introduced the term phase-transfer catalysis to explain the critical role of tetraalkylammonium or phosphonium salts (Q 1 X ) in the reactions between two substances located in different immiscible phases [1], For instance, the displacement reaction of 1-chlorooctane with aqueous sodium cyanide is accelerated many thousand-fold by the addition of hexadecyltributylphosphonium bromide 1 as a phase-transfer catalyst (Scheme 1.1). The key element of this tremendous reactivity enhancement is the generation of quaternary phosphonium cyanide, which renders the cyanide anion organic soluble and sufficiently nucleophilic. 

In the Michael-addition, a nucleophile Nu is added to the / -position of an a,fi-unsaturated acceptor A (Scheme 4.1) [1], The active nucleophile Nu is usually generated by deprotonation of the precursor NuH. Addition of Nu to a prochiral acceptor A generates a center of chirality at the / -carbon atom of the acceptor A. Furthermore, the reaction of the intermediate enolate anion with the electrophile E+ may generate a second center of chirality at the a-carbon atom of the acceptor. This mechanistic scheme implies that enantioface-differentiation in the addition to the yfi-carbon atom of the acceptor can be achieved in two ways (i) deprotonation of NuH with a chiral base results in the chiral ion pair I which can be expected to add to the acceptor asymmetrically and (ii) phase-transfer catalysis (PTC) in which deprotonation of NuH is achieved in one phase with an achiral base and the anion... 

Michael-aldol reaction as an alternative to the Morita-Baylis-Hillman reaction 14 recent results in conjugate addition of nitroalkanes to electron-poor alkenes 15 asymmetric cyclopropanation of chiral (l-phosphoryl)vinyl sulfoxides 16 synthetic methodology using tertiary phosphines as nucleophilic catalysts in combination with allenoates or 2-alkynoates 17 recent advances in the transition metal-catalysed asymmetric hydrosilylation of ketones, imines, and electrophilic C=C bonds 18 Michael additions catalysed by transition metals and lanthanide species 19 recent progress in asymmetric organocatalysis, including the aldol reaction, Mannich reaction, Michael addition, cycloadditions, allylation, epoxidation, and phase-transfer catalysis 20 and nucleophilic phosphine organocatalysis.21... 

Catalytic Michael additions of a-nitroesters 38 catalyzed by a BINOL (2,2 -dihydroxy-l,r-bi-naphthyl) complex were found to yield the addition products 39 as precursors for a-alkylated amino acids in good yields and with respectable enantioselectivities (8-80%) as shown in Scheme 9 [45]. Asymmetric PTC (phase transfer catalysis) mediated by TADDOL (40) as a chiral catalyst has been used to synthesize enantiomeri-cally enriched a-alkylated amino acids 41 (up to 82 % ee) [46], A similar strategy has been used to access a-amino acids in a stereoselective fashion [47], Using azlactones 42 as nucleophiles in the palladium catalyzed stereoselective allyla-tion addition, compounds 43 were obtained in high yields and almost enantiomerically pure (Scheme 9) [48]. The azlactones 43 can then be converted into the a-alkylated amino acids as shown in Scheme 4. 

Tanikaga and coworkers have reported the addition of nitroalkane anions to a-halo-a,P-unsaturated sulfoxides [72]. Further development of this work led to the use of nitroalkanes as alkyl group equivalents in conjugate addition to a,P-unsaturated sulfoxides [73-75]. Primary or secondary nitroalkanes such as 2-nitropropane (77), with DBU as a non-nucleophilic base, add to a,P-unsaturated sulfoxides including phenyl vinyl sulfoxide (26) to give products such as (78), which can be denitrated to yield (79) (Scheme 5.25). The Michael addition of nitroalkanes, and of diethyl N-acetylaminomalonate, to racemic phenyl vinyl sulfoxide using solid-liquid phase-transfer catalysis in the absence of solvent has also been accomplished [76]. 

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