Napper A D, Benkovic S J, Tramontano A, Lerner R A
Science. 1987 Aug 28;237(4818):1041-3. doi: 10.1126/science.3616626.
A monoclonal antibody elicited by a transition-state analog that is representative of an intramolecular six-membered ring cyclization reaction acted as a stereospecific, enzyme-like catalyst for the appropriate substrate. Formation of a single enantiomer of a delta-lactone from the corresponding racemic delta-hydroxyester was accelerated by the antibody by about a factor of 170, which permitted isolation of the lactone in an enantiomeric excess of about 94 percent. This finding demonstrates the feasibility of catalytic-antibody generation for chemical transformations that require stereochemical control.
由代表分子内六元环环化反应的过渡态类似物引发的单克隆抗体,对合适的底物起到了立体特异性的、类似酶的催化剂作用。该抗体使相应的外消旋δ-羟基酯形成单一对映体的δ-内酯的反应加速了约170倍,从而能够分离出对映体过量约94%的内酯。这一发现证明了针对需要立体化学控制的化学转化生成催化抗体的可行性。