α-杂原子取代烯碳的对映选择性转移反应

Symmetry Pub Date : 2024-09-06 DOI:10.3390/sym16091171
Mingyao Huang, Wenjing Shi, Lu Li
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引用次数: 0

摘要

人们普遍认为,金属碳烯是一类高效的中间体,可促进原本无法实现的转化。近几十年来,碳烯化学取得了长足的进步,在形成各种化学键和合成结构独特的分子方面表现出了非凡的能力。然而,这一领域的大部分研究都集中在 α 碳取代的碳烯上,而对结构种类更多的功能化碳烯,特别是那些被杂原子(如 O、N、P、S、Si、Ge、Sn 和 B)取代的碳烯的研究则相对较少。本综述旨在阐明涉及被这些元素取代的金属碳烯的对映选择性转移反应的进展,从而突出它们对扩大碳烯在当代化学中的结构多样性和合成用途的贡献。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Enantioselective Transfer Reactions of α-Heteroatom-Substituted Carbenes
Metal carbenes are widely acknowledged as a category of highly effective intermediates that facilitate otherwise inaccessible transformations. In recent decades, carbene chemistry has made considerable advances and has demonstrated remarkable abilities in the formation of diverse chemical bonds and the synthesis of structurally distinctive molecules. Nevertheless, the majority of research within this field has concentrated on α-carbon-substituted carbenes, with comparatively little investigation of carbenes that have been functionalized with a wider structural variety, particularly those that have been substituted with heteroatoms (e.g., O, N, P, S, Si, Ge, Sn and B). The objective of this review is to elucidate the advancements in enantioselective transfer reactions involving metal carbenes substituted with these elements, thereby highlighting their contribution to the expansion of the structural diversity and synthetic utility of carbenes in contemporary chemistry.
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