Tetrabutylammonium reductions with

Deoxy-l-fluoro-L-glycerol (18) has been prepared by, among other methods, the treatment of 3,4-0-benzylidene-2,5-0-methylene-l,6-di-O-p-tolylsulfonyl-D-mannitol107 (17) with tetrabutylammonium fluoride in acetonitrile, followed by removal of the benzylidene group, periodate oxidation, reduction with borohydride, and hydrolysis. 1,6-Dideoxy-l,6-difluorogalactitol108 was obtained by treatment of 2,3 4,5-di-0-isopropylidene-l,6-di-0-(methylsulfonyl)galactitol with tetra-... 

Chlorophenyl)glutarate monoethyl ester 87 was reduced to hydroxy acid and subsequently cyclized to afford lactone 88. This was further submitted to reduction with diisobutylaluminium hydride to provide lactol followed by Homer-Emmons reaction, which resulted in the formation of hydroxy ester product 89 in good yield. The alcohol was protected as silyl ether and the double bond in 89 was reduced with magnesium powder in methanol to provide methyl ester 90. The hydrolysis to the acid and condensation of the acid chloride with Evans s chiral auxiliary provided product 91, which was further converted to titanium enolate on reaction with TiCI. This was submitted to enolate-imine condensation in the presence of amine to afford 92. The silylation of the 92 with N, O-bis(trimethylsilyl) acetamide followed by treatment with tetrabutylammonium fluoride resulted in cyclization to form the azetidin-2-one ring and subsequently hydrolysis provided 93. This product was converted to bromide analog, which on treatment with LDA underwent intramolecular cyclization to afford the cholesterol absorption inhibitor spiro-(3-lactam (+)-SCH 54016 94. 

An alternative procedure is to convert the carbonyl compound into the toluene-p-sulphonylhydrazone,12 followed by reduction with either sodium borohydride in acetic acid,13 or with catecholborane, followed by decomposition of the intermediate with sodium acetate or tetrabutylammonium acetate.14 The former method is illustrated by the conversion of undecan-6-one into undecane (Expt 5.6), and the latter by the conversion of acetophenone into ethylbenzene (Expt 6.4, Method B). A feature of these methods is that with a, / -unsaturated ketones, migration of the carbon-carbon multiple bond occurs thus the tosylhydrazone of isophorone gives 3,3,5-trimethylcyclohex-l-ene, and the tosylhydrazone of oct-3-yn-2-one gives octa-2,3-diene. 

The allyl glycoside of a-D-Abe-(l ->3)-a-D-Man 115 was prepared by a different approach.200 The ethyl 1-thio-D-abequopyranoside donor 113 was obtained from methyl (3-D-galactopyranoside derivative 110 according to Scheme 33. The cyclic sulfate intermediate 111 was the precursor for the stereoselective reduction with tetrabutylammonium borohydride to 112 which was further derivatized to the thioglycosyl donor 113. Donor 113 was reacted with acceptor 114 to give 115 after deprotection. 

Deposition of platinum metal In the case of platinum no solid product was found. The ionic liquid darkened more and faster the smaller the distance between the surface of the ionic liquid [EMIM][TfO] containing tetrabutylammonium hexachloro-platinate ([n-Bu4N]2[PtCl6]) and the Ar/H2-plasma (3 1, overall pressure 100 Pa) was chosen. So far no other ionic liquid has been tested. The rate constant for the reduction of the tetrabutylammonium ion with a hydrated electron is only 1.4 x 106 LmoH1 s 1, hence the main rival pathway for reduction of platinum(IV) is the reduction of the imidazolium ion of the ionic liquid. As in the case of copper, a suitable platinum salt - maybe made by electro-oxidation of metallic platinum in a suitable ionic liquid - has to be found. 

Diastereoselective reduction of ketones. Trialky Isilanes can reduce aldehydes and ketones in the presence of a catalytic amount of tetrabutylammonium fluoride in HMPT cf. reductions with activated hydrosilanes, II, 554). Under these conditions esters and nitriles are not reduced. The reaction is stereoselective. Thus 2-methylcyclohcxanone is reduced selectively to cA-2-methylcyclohexanol the cvT-selectivity depends on the bulkiness of the hydrosilanc, being highest (95%) with triphenylsilane. 

The air-sensitive Cp-substituted hydridovanadium complex is obtained by hydrogenolysis of the corresponding methyl derivative. The corresponding anionic compound is obtained by reduction of CpV(CO)4 with sodium and protonation with water (Scheme 64). Thus obtained [CpVH(CO)3] (106) is a useful one-electron reductant to reduce bromo- and iodoalkanes, bromoalkenes, and arylbromides in THF. Furthermore, acid chlorides are reduced to the aldehydes. A similar reduction with (106) is performed by using phase-transfer conditions in the presence of tetrabutylammonium hydrogen sulfate. Nitro compounds and organic halides are reduced under these conditions. 

On the other hand, these values are dramatically modified if the presence of alkali-metal (sodium) counterions is taken into account, the ion-paired trianions becoming by far the most stable species (E = —4.5 eV). On this basis, it has been postulated that in the butoxide reduction of 65 and 67 formation of the potassium ion-paired trianions would be favored over that of the ion-paired monoanions, while reduction with tetrabutylammonium borohydride in THF or the electro-... 

Reduction (electrochemical or metals ) of dibromodifluoromethane produces difluorocarbene (carbenoid) which reacts with alkenes to form 1,1-difluorocyclopropanes. Electrochemical reduction was carried out on a platinum electrode at 20 C, while metal reduction with lead in the presence of tetrabutylammonium bromide (TBAB) in various solvents was carried out at 40-60°C. In both cases 1,1-difluorocyclopropanes were formed in moderate yield (Houben-Weyl, Vol. E19b, p 1475). 

Fraga et al. [1] smdied the reduction effect of another uncommonly used reductive agent tetrabutylammonium borohydride (NBU4BH4) on similar substrates as well. They found that substrate 3.19 was converted to cts-product 3.20b and trans-product 3.20a under tetrabutylammonium borohydride with 89 % yield (Fig. 3.7). The proportion was 8.2 1. The cis-product was the main product. 

Electrochemical reduction of a number of steroidal nuclear ketones at a stirred Hg-cathode affords the equatorial epimeric alcohol with a high degree of stereospecificity and in good yield comparable to reduction with Na in alcohol.—E 22a,5-Allospirostane-3, 12) -diol-ll-one diacetate electrolyzed in a catholyte soln. of tetrabutylammonium bromide in alcohol-water with a Hg-cathode and a carbon anode in an anolyte soln. of tetrabutylammonium chloride and tetrabutylammonium hydroxide in alcohol-water at —2.6 v. 22a,5-allospirostane-3j, ll -diol. Y 97%. F. e., reduction of ketones and a-hydroxyketones, and limitations s. P. Kabasakalian et al., J. Org. Chem. 26, 1738 (1961). 

Tetrabutylammonium iodide in trifluoroacetic anhydride is an effective reducing reagent [dS] This system can be used for direct reduction of arenesulfonic acids to the corresponding thiols or disulfides m moderate yields under mild conditions (equation 18) Alkanesulfonic acids are reduced by this system to disulfides with 30-57% yields [dfi]... 

Cyano-de-diazoniations of the Sandmeyer type have been used for the synthesis of aromatic nitriles for many decades (example Clarke and Reed, 1964), as cyanide ions are comparable to bromide and iodide in many respects. A homolytic cyano-de-diazo-niation that does not use metal ions as reductant or ligand transfer reagent was described by Petrillo et al. (1987). They showed that substituted diazosulfides (XC6H4 — N2 — SC6H5), either isolated or generated in situ from arenediazonium tetrafluoroborates and sodium benzenethiolate, react with tetrabutylammonium cyanide in dimethylsulfoxide under photon stimulation, leading to nitriles (XC6H4CN). The method worked well with eleven benzenediazonium ions substituted in the 3- or 4-position, and was also used for the synthesis of phthalo-, isophthalo-, and tere-... 

A similar reduction of nitrobenzene with (Me3Si)2Hg to give azobenzene and azoxybenzene has been described [86]. The dehydration of tetrabutylammonium fluoride di- or trihydrate by hexamethyldisilane 857 is discussed in Chapter 13. 

The selective reduction of the D-ring olefin in 106 using a partially poisoned catalyst (Pd/C, 0.25 % pyridine) provided intermediate 107 (83 %), which was epimerized at -78 °C with sodium methoxide (HOAc quench at -78 °C, 89 %) (Scheme 10.9). Deoxygenation by means of tosyl hydrazone 108 and subsequent treatment with catechol borane and tetrabutylammonium acetate gave pentacyclic... 

The electrochemical generation of the germyl anion has been the subject of a recent paper105. Evidence for its formation by SET reduction of Ph3GeH on Pt in DMF with tetrabutylammonium tetrafluoroborate is based on 13C NMR which shows a strong down-field shift of Ca 30 ppm for the ipso carbon of the anion. The anion tends to yield Ph3GeGePh3 above 20 °C, but is also trapped by reactions at —40°C with O2 and CH3I ... 

The efficiency of the [2 + 2]-cycloadditions of 417 was utilized in a strategy for the synthesis of cephalosporin derivatives that carry an acetone or acetic acid ester group in the 3-position (Scheme 6.88) [175]. Liberated in the presence of 2-(trimethylsilyl-oxy)propene, 417 underwent cycloaddition leading to 435, treatment of which with tetrabutylammonium or hydrogen fluoride furnished the A3-cephalosporin 436 admixed with the A2-isomer. This mixture was converted to pure 436 by an oxidation-reduction sequence. In addition to the trimethylsilylenol ether of acetone, the... 

Obtained in acetonitrile solution containing 0.2 mol dm-3 BuJNBF4 as supporting electrolyte. Solutions were 1 X 10 3moldm-3 in ligand and potentials were obtained with reference to Ag/Ag+ electrode. "Cathodic shift in reduction potential produced by presence of anions (up to 10 equiv) added as their tetrabutylammonium salts. 

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