Advances in the Catalytic Asymmetric Synthesis of Chiral Spiroketals

被引:6
作者
Yan Hui
Zhang Man
Li Lin
Hu Teng
Yang Wulin [1 ]
机构
[1] East China Univ Sci & Technol, Shanghai Key Lab Chem Biol, Shanghai 200237, Peoples R China
基金
中国国家自然科学基金;
关键词
asymmetric catalysis; enantioselectivity; spiroketals; BETA-ALKYNYL KETONES; ENANTIOSELECTIVE SYNTHESIS; BENZANNULATED SPIROKETALS; DIVERGENT SYNTHESIS; NATURAL-PRODUCTS; A-C; GOLD; ACID; SPIRO; SPIROACETALS;
D O I
10.6023/cjoc202205001
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
As an unique spiro skeleton, spiroketals are ubiquitous motifs in many natural products, biologically active molecules, and privileged chiral ligands. The development of efficient synthetic methods for the preparation of spiroketals has long been a hot research topic in organic synthesis. In particular, the remarkable advances regarding the catalytic asymmetric synthesis of chiral spiroketals have been achieved over the past decade. The progress in the field of catalytic asymmetric synthesis of chiral spiroketals is summarized according to the reaction types. The future development direction of this field is also prospected.
引用
收藏
页码:3640 / 3657
页数:18
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