New cycloaddition/fragmentation strategies for preparing 5-7-5 and 5-7-6 fused tricyclic ring systems

被引:0
|
作者
He, Jing [1 ]
Snapper, Marc L. [1 ]
机构
[1] Boston Coll, Merkert Chem Ctr, Dept Chem, Chestnut Hill, MA 02467 USA
关键词
Cyclobutadiene; Cycloaddition; Intramolecular; Cyclopropanation; Fragmentation; TUMOR PROMOTERS; PHORBOL; FRAGMENTATION; CYCLOADDITION; REARRANGEMENT; SKELETON;
D O I
10.1016/j.tet.2013.05.129
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Tethering additional functionality to cyclobutadienyl iron tricarbonyl complexes provides new opportunities for the rapid construction of medium-ring-containing polycyclic compounds. Specifically, an intramolecular cycloaddition between cyclobutadiene and a tethered olefin, followed by an intramolecular cyclopropanation of the resulting cyclobutene-containing adduct generates highly strained pentacyclic intermediates. These compounds can then be relaxed thermally to generate 5-7-5 and 5-7-6 fused tricyclic ring systems that are shared with numerous natural products. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:7831 / 7839
页数:9
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