NXS, Morpholine, and HFIP: The Ideal Combination for Biomimetic Haliranium-Induced Polyene Cyclizations

被引:95
作者
Arnold, Andreas M. [1 ,2 ]
Poethig, Alexander [2 ]
Drees, Markus [2 ]
Gulder, Tanja [1 ,2 ]
机构
[1] Tech Univ Munich, Dept Chem, Biomimet Catalysis, Lichtenbergstr 4, D-85748 Garching, Germany
[2] Tech Univ Munich, Catalysis Res Ctr, Ernst Otto Fischer Str 1, D-85748 Garching, Germany
关键词
OCCURRING ORGANOHALOGEN COMPOUNDS; BIOGENETIC-TYPE SYNTHESIS; MARINE NATURAL-PRODUCTS; HYDROGEN-BOND DONOR; BROMINATIVE CYCLIZATION; FLUORINATED ALCOHOLS; ENANTIOSELECTIVE BROMOCYCLIZATION; ANTIBIOTICS NAPYRADIOMYCINS; SELECTIVE BROMOCYCLIZATION; ANTIMUTAGENIC AGENTS;
D O I
10.1021/jacs.8b00113
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In contrast to Nature that accomplishes polyene cyclizations seemingly with ease, such transformations are difficult to conduct in the lab. In our program dealing with the development of selective halogenations of alkenes, we now asserted that standard X+ reagents are perfectly suited for the biomimetic cation-pi cyclization of both electron rich and poor linear polyenes in the presence of the Lewis base morpholine and the Lewis acid HFIP. The method stands out due to its broad substrate scope and practicability together with high chemical yields and excellent selectivities, even for highly challenging chloriranium-induced polyene cyclizations.
引用
收藏
页码:4344 / 4353
页数:10
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