2-Pyridylcarboxylates

Sometimes, instead of using protecting groups as chemoselective control elements it may be more convenient to resort to activating groups as, for instance, the S-2-pyridylcarboxylic esters (24) which react intramolecularly to give macrolides 25 in excellent yields [20] (Scheme 12.7). 

The kinetics of concerted thermal elimination reactions of a series of ethyl (hetero) arylcarboxylate esters (2-thienyl-, 3-thienyl-, 2-furyl, 3-furyl, 4-pyridyl-, 3-pyridyl-, and 2-pyridylcarboxylate) in the gas phase seem to indicate that there is little charge separation in the transition state (83) this is in contrast with the behaviour of the corresponding /-butyl and isopropyl esters for which a semi-concerted transition state (82) was proposed previously.49 Results of a kinetic study of the gas-phase elimination reactions of methylbenzoyl formate (84) and 3-hydroxy-3-methylbutan-2-one (85) have been compared with those for pyruvic acid (87) and benzoylformic acid (86).50 The relative rates of reaction [(86)/(87) 46, (87)/(85) = 1.1 x 105 and (86)/(82) = 1 x 106] reveal that the acidity of the hydrogen atom involved in the elimination process, rather than the initial polarization of the C—C bond which undergoes cleavage, is the important rate-controlling factor. 

TT-Allylnickel halides react with 2-pyridylcarboxylates as acylating agents in a new mild process leading to /3,y-unsaturated ketones/ and the oxidative rearrangement of tertiary cyclopropylcarbinols provides a further route to /3,y-unsaturated ketones, if only in moderate yields [equation (22)]. 

Similarly, triphenyltin nicotinate (3-pyridylcarboxylate), Ph3SnOOCCeH4N, forms supramolecular chain-like arrays, 130, with Sn-O 2.137 A and Sn -N 2.568 A [303]. 

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