Aldehydes acid halide synthesis

The enolate reactivity associated with this approach to C-glycoside synthesis was, however, first developed with octulosonic acid derivatives, such as 283 [114], 284 [115], and 285 [116], and a series of examples involving aldehyde and halide-based electrophiles are shown in Scheme 74. Related studies involving stereoselective protonation of this class of exocyclic enolate have also been described [13] and Scheme 75 illustrates this with an example of reductive samariation (using ethane-1,2-diol, but no HMPA) of an anomeric acetate 286 [117]. 

Alternative methods for the synthesis of peptide aldehydes include reduction of acid halides, phenyl esters, thioesters, and anhydrides prepared from corresponding acids, isoxazolidides, and the hydrolysis of thiazolidine peptides 17,54-56 Enzymes such as thermolysin, subtilisin, and pronase E have proven valuable as effective semisynthetic alternatives 40,57 5 62 ... 

Reduction of acid halides with lithium tri-tert-butoxyaluminum hydride is an effective method for synthesis of amino aldehydes. Nonfunctionalized amino aldehydes 22 are readily prepared from respective reduction of the N-terminal Fmoc, Boc, or Z acid chlorides or fluorides 21 (Scheme 8, Table 9). This method afforded these aldehydes in about 60% yield with small differences in optical rotation as compared to literature values 11,33 48 54 55 ... 

Hydrolysis yields the terminal acetylene (3) carbonation yields the propargylic acid (4). Synthesis of a wide variety of acetylenes is possible by the reaction of the intermediate lithium acetylides with other electrophiles (alkyl halides, aldehydes, ketones). 

Samarium acyl anions can be trapped by electrophiles other than acid halides. For example, addition of a mixture of a carboxylic acid chloride and an aldehyde or ketone to a solution of Sml2 in THF results in the synthesis of a-hydroxy ketones (equations 78 and 79). Intramolecular versions of the reaction have also been performed, although the scope of the reaction is limited owing to the difficulty in obtaining suitable substrates for the reaction (equation 80). ... 

Notable examples of general synthetic procedures in Volume 47 include the synthesis of aromatic aldehydes (from dichloro-methyl methyl ether), aliphatic aldehydes (from alkyl halides and trimethylamine oxide and by oxidation of alcohols using dimethyl sulfoxide, dicyclohexylcarbodiimide, and pyridinum trifluoro-acetate the latter method is particularly useful since the conditions are so mild), carbethoxycycloalkanones (from sodium hydride, diethyl carbonate, and the cycloalkanone), m-dialkylbenzenes (from the />-isomer by isomerization with hydrogen fluoride and boron trifluoride), and the deamination of amines (by conversion to the nitrosoamide and thermolysis to the ester). Other general methods are represented by the synthesis of 1 J-difluoroolefins (from sodium chlorodifluoroacetate, triphenyl phosphine, and an aldehyde or ketone), the nitration of aromatic rings (with ni-tronium tetrafluoroborate), the reductive methylation of aromatic nitro compounds (with formaldehyde and hydrogen), the synthesis of dialkyl ketones (from carboxylic acids and iron powder), and the preparation of 1-substituted cyclopropanols (from the condensation of a 1,3-dichloro-2-propanol derivative and ethyl-... 

When arylhydrazones of aldehydes or ketones are treated with a catalyst, elimination of ammonia takes place and an indole is formed, in the Fischer indole synthesis,Zinc chloride is the catalyst most frequently employed, but dozens of others, including other metal halides, proton and Lewis acids, and certain transition metals have also been used. Microwave irradiation has been used to facilitate this reaction. Aniline derivatives react with a-diazoketones, in the presence of a... 

Carbon monoxide rapidly inserts into the carbon—zirconium bond of alkyl- and alkenyl-zirconocene chlorides at low temperature with retention of configuration at carbon to give acylzirconocene chlorides 17 (Scheme 3.5). Acylzirconocene chlorides have found utility in synthesis, as described elsewhere in this volume [17]. Lewis acid catalyzed additions to enones, aldehydes, and imines, yielding a-keto allylic alcohols, a-hydroxy ketones, and a-amino ketones, respectively [18], and palladium-catalyzed addition to alkyl/aryl halides and a,[5-ynones [19] are examples. The acyl complex 18 formed by the insertion of carbon monoxide into dialkyl, alkylaryl, or diaryl zirconocenes may rearrange to a r 2-ketone complex 19 either thermally (particularly when R1 = R2 = Ph) or on addition of a Lewis acid [5,20,21]. The rearrangement proceeds through the less stable... 

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