The Difference a Single Atom Can Make: Synthesis and Design at the Chemistry-Biology Interface

被引:48
|
作者
Boger, Dale L. [1 ,2 ]
机构
[1] Scripps Res Inst, Dept Chem, 10550 North Torrey Pines Rd, La Jolla, CA 92037 USA
[2] Scripps Res Inst, Skaggs Res Inst, 10550 North Torrey Pines Rd, La Jolla, CA 92037 USA
来源
JOURNAL OF ORGANIC CHEMISTRY | 2017年 / 82卷 / 23期
关键词
ACID AMIDE HYDROLASE; DNA ALKYLATION PROPERTIES; ALPHA-KETOHETEROCYCLE INHIBITORS; INTRAMOLECULAR DIELS-ALDER/1,3-DIPOLAR CYCLOADDITION; DIELS-ALDER REACTIONS; ALA-D-LAC; LEFT-HAND SUBUNIT; CC-1065 FUNCTIONAL ANALOGS; ASYMMETRIC TOTAL-SYNTHESIS; IN-SITU ACTIVATION;
D O I
10.1021/acs.joc.7b02088
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A Perspective of work in our laboratory on the examination of biologically active compounds, especially natural products, is presented. In the context of individual programs and along with a summary of our work, selected cases are presented that illustrate the impact single atom changes can have on the biological properties of the compounds. The examples were chosen to highlight single heavy atom changes that improve activity, rather than those that involve informative alterations that reduce or abolish activity. The examples were also chosen to illustrate that the impact of such single-atom changes can originate from steric, electronic, conformational, or H-bonding effects, from changes in functional reactivity, from fundamental intermolecular interactions with a biological target, from introduction of a new or altered functionalization site, or from features as simple as improvements in stability or physical properties. Nearly all the examples highlighted represent not only unusual instances of productive deep-seated natural product modifications and were introduced through total synthesis but are also remarkable in that they are derived from only a single heavy atom change in the structure.
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页码:11961 / 11980
页数:20
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