Adamantane-1-carboxylic acid

Dichloroquinoxaline gave 2-adamantyl-3-chloroquinoxaline (1-adamantane-carboxylic acid, AgN03, ( 4)28203, MeCN-H20, A, 80°C, 2h 47%). ... 

Traces of adamantane carboxylic acid also detected. 

Adamantane carboxylic acids 13, CM-/3, Me-p A-reciprocal 66 indirect detection (sodium chromate)... 

E-S Kwak, FA Gomez. Determination of the binding of f -cyclodextrin derivatives to adamantane carboxylic acids using capillary electrophoresis. Chromatographia 43 659-662, 1996. 

Conversion of the methyl ester of 1-adamantane carboxylic acid to 1-ada-mantyl dimethylcarbinol (66) by reaction with CH3Mgl followed by dehydration and subsequent hydrogenation provides a convenient route to 1-iso-propyladamantane (66a) 164> 20°). Simmons-Smith cyclopropanation of 1-isopropenyladamantane (67) followed by hydrogenolysis of the cyclopropane ring gives 1-r-butyladamantane (68) 204>. An alternative synthesis... 

Functional group manipulations are equally successful for the preparation of a wide variety of 2-substituted adamantanes. Starting with the methyl ester of 2-adamantane carboxylic acid S7> 2061, 2-t-butyladamantane (71) may be prepared in a manner anlogous to that described above for the synthesis of the bridgehead isomer (Scheme 17) 2M These reactions illustrate the... 

Table IS. Acidities of alkyl substituted adamantane carboxylic acids (see also Ref.4))...

Similar results are obtained when 19-nortestosterone and related androgens 346> as well as various nucleosides347 are esterified with adamantane carboxylic acids. Whereas 107 exhibits a long duration of myotropic activity coupled with significantly reduced androgenicity, the 3-methyl and 3,5-di-... 

Substituted adamantanes have been employed in the study of several reaction mechanisms. The Kolbe electrolyses of 1- and 2-adamantane carboxylic acids and 1- and 2-adamantyl acetic acids have been compared in detail. Car-bonium ion-derived products are observed from the electrolyses of both 1-adamantyl carboxylic acid and 1-adamantyl acetic acid. A mixture of radical and carbonium ion-derived products are obtained from 2-adamantyl carboxylic acid and mainly radical-derived products are obtained from 2-adamantyl acetic acid. These results parallel the known or expected stabilities of the intermediate carbonium ions 366 ... 

A suspension of betamethasone (740.0 mg) in dioxan (20 ml) was treated with adamantane carboxylic acid (1.96 g) and trifluorcacetic anhydride (0.75 ml). The mixture was stirred at room temperature for 23 h during which time the steroid completely dissolved. Addition of sodium bicarbonate (2.0 g) and water gave a waxy semi-solid which was separated from the supernatant liquid by decantation. Water and a little methanol were added to the solid and the resulting granular material was removed by filtration and washed well with water. Fractional crystallization from methanol afforded adamantane carboxylic anhydride as the less soluble component and betamethasone 21-adamantane-l -carboxylate as the more soluble component. 

Figure 33 Structures of (a) pivalic acid (b) 2,2-dimethylbutyric acid and (c) 1 -adamantane carboxylic acid.

PpyFess Pt(acac)2, Fe(CO)5 hexadecyl amine 1-adamantane- carboxylic acid 350-360 8 85, 86... 

Cinnamoyl- 6-CD (6-CiO-/3-CD) was sparingly soluble in water, although most 6-substituted 6-CDs are soluble. However, 6-CiO-/3-CD was solubilized in water on the addition of adamantane carboxylic acid or p-iodoaniline which could be included in a 6-CD cavity. These results suggest that 6-CiO-/l-CD formed supramolecular polymers in the solid state, as shown in the proposed structure in Fig. 17. The X-ray powder pattern of 6-CiO-/l-CD was similar to that of the complex between p-CD and ethyl cinnamate, in which /3-CDs formed a layer structure. The crystal structure of 6-aminocinnamoyl-/3-CD (6-aminoCiO-/l-CD) is shown in Fig. 12 and we discussed the relationship between crystal packing and the substituent group in Sect. 2.8. 

Figure 36.4 PEG-substituted CDs (6-PEC600acid-HyCiO-/3-CD) from PEC 600 diacid, dynamic exchange between PEG inclusion, and exclusion by adamantane carboxylic acid (AdCA).

The reaction of 1-adamantane carboxylic acid proceeded smoothly at 80 °C, providing Boc-protected amine 92 in high yield, but the slow step of the process was addition of the ert-butoxy nucleophile (butoxide or butanol) to the isocyanate intermediate. Of numerous catalysts and conditions screened to accelerate that addition, zinc triflate in tetrahydrofuran solvent proved optimal, allowing the process to occur smoothly at 40 °C for a range of alkyl carboxylic acids. In some cases, such as the stereoretentive conversion of or-methyl-y -siloxy propionic acid 93 to Boc-protected chiral amine 94, inclusion of additional tert-butanol was required. Catalysis was proposed to occur via an isocyanate-derived, zinc-complexed carbamoyl bromide. The Lebel conditions were also applied to malonate monoesters as a route to cr-disubstituted-cr-amino acids. 

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