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Gaining Insight Into Reactivity Differences Between Malonic Acid Half Thioesters (MAHT) and Malonic Acid Half Oxyesters (MAHO)
Author(s) -
Bew Sean P.,
Stephenson G. Richard,
Rouden Jacques,
Godemert Jeremy,
Seylani Haseena,
MartinezLozano Luis A.
Publication year - 2017
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.201605148
Subject(s) - malonic acid , chemistry , thioester , thiophenol , hydrogen–deuterium exchange , deuterium , enol , methanol , reactivity (psychology) , medicinal chemistry , hydrogen , organic chemistry , catalysis , medicine , physics , alternative medicine , pathology , quantum mechanics , enzyme
An efficient two‐step synthesis of structurally and functionally diverse thiophenol‐ and (cyclo)alkyl‐derived malonic acid half thioesters (MAHTs) and phenol‐derived malonic acid half oxyesters (MAHOs) has been achieved using cheap, readily available and easily handled starting materials. The synthesis of the MAHTs and MAHOs (the majority of which have not been previously reported) is readily scalable to afford gram quantities of product. In a hydrogen → deuterium exchange, an interesting stereoelectronic effect was observed when different aryl groups were incorporated. Significant changes in the rates of hydrogen → deuterium exchange and levels of isotope incorporation were observed. By way of example, using [ 2 H]methanol and 4‐bromophenol‐derived MAHO afforded only 14 % [ 2 H]‐incorporation (9 min, k =31) whereas the corresponding 4‐bromothiophenol‐derived MAHT afforded 97 % [ 2 H]‐incorporation (9 min, k =208). In a benchmark procedure and comprehensive DFT study, 54 ester and thioester configurations and conformations were characterized. In the MAHT series, a sulfur‐containing molecular orbital provides a path for increased delocalisation of electron density into the enol that is unavailable in MAHOs. This facilitates keto–enol tautomerisation and consequently enhances the rate and percentage of hydrogen → deuterium exchange.