A Diels-Alder/Retro-Diels-Alder Approach for the Enantioselective Synthesis of Microbial Butenolides

被引:22
|
作者
Citron, Christian A. [1 ]
Wickel, Susanne M. [1 ]
Schulz, Barbara [2 ]
Draeger, Siegfried [2 ]
Dickschat, Jeroen S. [1 ]
机构
[1] Tech Univ Carolo Wilhelmina Braunschweig, Inst Organ Chem, D-38106 Braunschweig, Germany
[2] Tech Univ Carolo Wilhelmina Braunschweig, Inst Mikrobiol, D-38106 Braunschweig, Germany
关键词
Synthetic methods; Diels-Alder reaction; Natural products; Lactones; GAMMA-HYDROXYBUTYRIC ACID; MORPHOLOGICAL DEVELOPMENT; SECONDARY METABOLISM; BIOSYNTHESIS; VOLATILES; PHEROMONE; FUNGI;
D O I
10.1002/ejoc.201200991
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Several volatile lactones have been identified from the endophytic fungus Geniculosporium sp. isolated from the rockrose Cistus monspeliensis, commonly known as Montpelier cistus. The fungal volatiles were collected from agar-plate cultures by using a closed-loop stripping apparatus and the headspace extracts were analysed by GCMS. Structures for these lactones were proposed from their mass spectral data. The suggested structures were verified by synthesis of reference compounds through a DielsAlder/retro-DielsAlder approach. This synthetic method was also successfully applied in the synthesis of butenolides that are signalling molecules from streptomycetes. For the enantioselective synthesis of these butenolides a modified route including an enantioselective DielsAlder reaction was used.
引用
收藏
页码:6636 / 6646
页数:11
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