首页> 外文期刊>Current Organic Chemistry >The Catalytic Enantioselective Synthesis of Optically Active Epoxides and Tetrahydrofurans.Asymmetric Epoxidation, the Desymmetrization of meso-Tetrahydrofurans, and Enantiospecific Ring-Enlargement
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The Catalytic Enantioselective Synthesis of Optically Active Epoxides and Tetrahydrofurans.Asymmetric Epoxidation, the Desymmetrization of meso-Tetrahydrofurans, and Enantiospecific Ring-Enlargement

机译:光学活性环氧化物和四氢呋喃的催化对映选择性合成不对称环氧化,中四氢呋喃的不对称化和对映体环扩大

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Recent developments in metallosalen-catalyzed asymmetric oxidation, namely, the epoxidation of simple olefins and the desymmetrization of meso-tetrahydrofurans by using second-generation metallosalen complexes are discussed. As an alternative approach, the enantiospecific ring-enlargement of oxetanes for preparing optically active tetrahydrofurans is also described.nnOxygen heterocycles such as epoxides and tetrahydrofurans occur in a wide variety of natural products where their configurations often play an important role in defining biological activity. Furthermore, these oxygen heterocycles can serve as versatile chiral building blocks for the enantiospecific synthesis of various compounds. Obviously, methods for the stereocontrolled synthesis of epoxides and tetrahydrofurans will be of great value for organic synthesis. Accordingly, during the last two decades the development of new methodologies for the stereoselective synthesis of this class of compounds from readily available starting materials has been a major objective in organic synthesis as attested by numerous publications. As a result, many efficient catalysts and reagents have been devised and high enantioselectivities achieved for synthesizing oxygen heterocycles. Examples are chiral titanium-tartrate (1,2), metalloporphyrins (3), (salen)manganese complexes (4,5,6), ketones (via dioxiranes) (7), and iminium salts (via oxaziridinium salts), for achieving epoxidation with high enantioface-selectivity. Moreover, the desymmetrization of meso-heterocycles has been effected with (salen)manganese complexes (4). In the present review, we describe some recent developments in metallosalen-catalyzed asymmetric epoxidation and the desymmetrization of meso-tetrahydrofurans and related compounds. In addition, the enantiospecific ring-enlargement of oxetanes to tetrahydrofurans is briefly described.
机译:讨论了金属硅铝烯催化的不对称氧化的最新进展,即使用第二代金属硅铝烯配合物的简单烯烃的环氧化和内四氢呋喃的脱对称。作为替代方法,还描述了用于制备旋光四氢呋喃的氧杂环丁烷的对映体特异性环扩大。氧合杂环如环氧化物和四氢呋喃存在于多种天然产物中,它们的构型通常在定义生物活性中起重要作用。此外,这些氧杂环可用作各种化合物的对映体特异性合成的通用手性构件。显然,立体控制合成环氧化物和四氢呋喃的方法对于有机合成将具有重要的价值。因此,在过去的二十年中,由许多出版物证明,从容易获得的起始原料立体选择性合成这类化合物的新方法学的发展已成为有机合成的主要目标。结果,已经设计出许多有效的催化剂和试剂,并获得了用于合成氧杂环的高对映选择性。例子有手性酒石酸钛(1,2),金属卟啉(3),(锰)锰络合物(4,5,6),酮(通过二恶英)(7)和亚胺盐(通过恶二叠氮盐)。具有高对映体选择性的环氧化。此外,中(杂环)锰配合物已经实现了中杂环的不对称化(4)。在本综述中,我们描述了金属硅铝催化的不对称环氧化和中四氢呋喃及相关化合物的脱对称化的一些最新进展。另外,简要描述了氧杂环丁烷对映体环扩大为四氢呋喃。

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