Propellanes-From a Chemical Curiosity to "Explosive" Materials and Natural Products

被引:185
作者
Dilmac, Alicia M. [1 ]
Spuling, Eduard [1 ]
de Meijere, Armin [2 ]
Braese, Stefan [1 ,3 ]
机构
[1] Karlsruhe Inst Technol, Inst Organ Chem, Fritz Haber Weg 6, D-76131 Karlsruhe, Germany
[2] Georg August Univ Gottingen, Inst Organ & Biomol Chem, Tammannstr 2, D-37077 Gottingen, Germany
[3] Karlsruhe Inst Technol, Inst Toxicol & Genet, Eggenstein Leopoldshafen, Germany
关键词
functional materials; natural products; pharmacological activity; propellanes; staffanes; ENANTIOSELECTIVE TOTAL SYNTHESES; TINKERTOY CONSTRUCTION SET; ALPHA-ALKYNONE CYCLIZATION; PHASE-TRANSFER CATALYSTS; CARBON-CARBON BOND; INFLUENZA-A VIRUS; M2; ION-CHANNEL; GC-MS ANALYSIS; ESSENTIAL OIL; BENZOANNELATED CENTROPOLYQUINANES;
D O I
10.1002/anie.201603951
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Propellanes are a unique class of compounds currently consisting of well over 10 000 representatives, all featuring two more or less inverted tetrahedral carbon atoms that are common to three bridging rings. The central single bond between the two bridgeheads is significantly weakened in the smaller entities, which leads to unusual reactivities of these structurally interesting propeller-like molecules. This Review highlights the synthesis of such propellanes and their occurrence in material sciences, natural products, and medicinal chemistry. The conversion of [1.1.1]propellane into bridgehead derivatives of bicyclo[1.1.1]pentane, including oligomers and polymers with bicyclo[1.1.1]penta-1,3-diyl repeat units, is also featured. A selection of natural products with larger propellane subunits are discussed in detail. Heteropropellanes and inorganic propellanes are also addressed. The historical background is touched in brief to show the pioneering work of David Ginsburg, Gunther Snatzke, Kenneth B. Wiberg, Gunter Szeimies, and others.
引用
收藏
页码:5684 / 5718
页数:35
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