2 edition of Stereospecific synthesis of chiral 1,2-diaryl-1,2-diaminoethanes by controlling diaza-Cope rearrangement reactions with resonance-assisted hydrogen bonds. found in the catalog.
Stereospecific synthesis of chiral 1,2-diaryl-1,2-diaminoethanes by controlling diaza-Cope rearrangement reactions with resonance-assisted hydrogen bonds.
Written in English
Resonance-assisted hydrogen bonds (RAHBs) are a class of unusually short, strong hydrogen bonds as revealed by the seminal work of Gilli et al. Over the years, it has been a challenge to demonstrate large effects with hydrogen bonds in kinetics and thermodyamics of chemical reactions. This thesis reports the influence of RAHBs on kinetics and thermodynamics of diaza-Cope rearrangement reactions and their applicability in stereospecific synthesis of d,l-1,2-diaryl-1,2-diaminoethanes.Chapter 1 is a general overview on the applications of vicinal diamines in asymmetric catalysis and medicinal chemistry and some literature reported methodologies of their synthesis. In Chapter 2 the role of RAHBs in the highly selective formation of N,N"-disalicylidene- meso-1,2-bis(2-methoxyphenyl)ethylenediamine (88) over N,N"-bis(2-methoxyphenyl)-meso-1,2-bis(2-hydroxyphenyl)ethylenediamine (87) via diaza-Cope rearrangement is demonstrated. The presence of RAHBs in compound 88 was confirmed by 1H NMR (deltaO-H = 13.39 ppm) and X-ray crystallography (N···HO distance of about 2.61 A). Furthermore, DFT computation at the B3LYP/6-31++G(d,p) level showed the RAHBs in compound 88 are about twice as strong as normal hydrogen bonds in compound 87. The effect of RAHBs on the rate of diaza-Cope rearrangements was investigated (reactions 3--5 on p 63). The formation of RAHBs stabilized product increased the rate by about 40 times compare to the product without hydrogen bonds.In Chapter 3 the knowledge gained from understanding the effect of RAHBs on the diaza-Cope rearrangement is applied to stereospecific synthesis of symmetrical d,l-1,2-diaryl-1,2-diaminoethanes 146, 147, 152, 153 and unsymmetrical d,l-1,2-diaryl-1,2diaminoethanes 151 and 154 from d,l-1,2-bis(2-hydroxyphenyl)ethylenediamine. Chapter 4 describes the explorations for novel methods to prepare d,l-1,2-bis(2-hydroxyphenyl)-ethylenediamine.
|The Physical Object|
|Number of Pages||164|
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