Titanium chloride-Sodium borohydride

Other reagents which have occasionally been used to cleave hydrazides include diborane (which also reduces the carbonyl groups), sodium naphthalenide, 0,0-diethyldithiophosphoric acid, (EtO)2PS2H, - and sulfur monochloride. Nickel-aluminum alloy in aqueous methanolic potassium hydroxide is a good reagent for reductively cleaving a number of N—N bonded compounds, such as A -methyl-A -phenylhydrazine and Af/Z-dimethylnitrosamine. - Nitrosamines have also been cleaved with titanium(IV) chloride-sodium borohydride and lithium aluminium hydride. 

N-OXIDES Diphosphorus tetraiodide. Hexachlorodisilane. Molybdenum(V) chloride-Zinc. Titanium(IV) chloride-Sodium borohydride. 7... 

Carbonyl Group Reduction. The flow of new methods for reduction of acid derivatives and aldehydes or ketones to alcohols continues unabated. The Report last year (4,134) featured the sodium borohydride reduction of carboxylic acid derivatives, originally thought to be 2-thiazoline-2-thiol esters (14), to give alcohols in good yields. Full details of the method have now appeared (Scheme 8), and it seems that the acid derivatives are in fact the 3-acyl thiazolidine-2-thiones (IS) dissappearance of their yellow colour is an easy way to monitor the reduction. Carboxylic acids or their chlorides can also be reduced to primary alcohols in good yields at room temperature using a titanium tetrachloride-sodium borohydride combination. ... 

Tertiary amine TV-oxides are rapidly deoxygenated by carbon disulphide1112. Oximes are reduced to primary amines by titanium(III) chloride in the presence of sodium cyanoborohydride, NaBTpCN1. The combined action of sodium borohydride and a chiral... 

As noted earlier, most classical antidepressant agents consist of propylamine derivatives of tricyclic aromatic compounds. The antidepressant molecule tametraline is thus notable in that it is built on a bicyclic nucleus that directly carries the amine substituent. Reaction of 4-phenyl-l-tetralone (18) (obtainable by Friedel-Crafts cyclization of 4,4-diphenyl butyric acid) with methyl amine in the presence of titanium chloride gives the corresponding Schiff base. Reduction by means of sodium borohydride affords the secondary amine as a mixture of cis (21) and trans (20) isomers. The latter is separated to afford the more active antidepressant of the pair, tametraline (20). 

Reduction of l,2,4-triazin-3-ones (84) with Raney nickel, zinc and acetic acid, lithium aluminum hydride, sodium borohydride, titanium(III) chloride, p-toluenethiol, hydrogen and a palladium catalyst, or electrochemically, produces 4,5-dihydro-l,2,4-triazin-3-ones (268) (78HC(33)189, p. 246, 80JHC1237), which may be further reduced to 1,4,5,6-tetrahydro-l,2,4-triazin-3-ones (269). l,2,4-Triazin-3-ones (84) with hydriodic acid and phosphorus yielded imidazoles (05LA(339)243). 3-Alkoxy-l,2,4-triazines (126) and sodium borohydride gave the 2,5-dihydro derivatives (270) (80JOC4594). 

Titanium(II) reagents have also been used to reduce aliphatic nitro compounds to amines halo, cyano and ester groups are not reduced. Sodium borohydride, in the presence of catalytic amounts of nickel(II) chloride, reduces a variety of aliphatic nitro compounds to amines. Nickel boride (Ni2B) is an active catalyst for reductions of primary, secondary and tertiary nitro aliphatic compounds to amines. The reduction of nitrocyclohexane (45) yields cyclohexylamine (47) as well as small amounts of dicyclohexylamine (49), the latter being formed via reaction of intermediates (46) and (48 equation 28). 

Dialkylpyrrolines are reduced by diisobutylaluminum hydride stereospecifically to give m-tetrahydropyrroles with or without Lewis acid12. Lithium aluminum hydride alone, or in the presence of titanium(IV) chloride or trimethyl aluminum, also reduces 2,5-dialkylpyrrolines to rL-tetrahydropyrroles. On the other hand, sodium borohydride gives an equal mixture of cis-and ran.v-tetrahydropyrroles, but in the presence of nickel(II) chloride or titanium(IV) chloride the major component obtained is always the cu-diastereomer12. 

Amino acid esters can be dimerized to dioxopiperazines, which are conveniently reduced with sodium borohydride,/titanium(IV) chloride to give the corresponding chiral piperazine derivatives. Thus, from valine and phenylalanine, useful auxiliaries 20 and 21 were obtained9, and used for the alkylation of carbanions (Section D. 1.1.1.3.1.) and as catalysts for the addition of zinc alkyls to aldehydes (Section D.1.3.1.4.), as well as for enantioselective deprotonation and elimination (Section C.). 

Sodium triacetoxyborohydride, 283 Titanium(III) chloride, 302 Tributyltin hydride, 316 Zinc borohydride, 167 of alkenes to alkanes (R)-(-F)- and (S)-(-)-2,2 -Bis(di-phenylphosphine)-l,1 -binaphthyl, 36 [1,4-Bis(diphenylphosphine)-butanej(cycloheptatriene)-rhodium(I) tetrafluoroborate, 89 [ 1,4-Bis(diphenylphosphine)butane]-(norbornadiene)rhodium(I) tetrafluoroborate, 37... 

Fluoromethyl phenyl sulfone, 135 Chlorohydrins Calcium borohydride, 62 Lithium, 157 Sodium nitrite, 282 Titanium(IV) chloride-1,8-Diazabi-cyclo[5.4.0]undecene-7, 309 Iodohydrins... 

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