Titanium-Mediated Domino Cross-Coupling/Cyclodehydration and Aldol-Addition/Cyclocondensation: Concise and Regioselective Synthesis of Polysubstituted and Fused Furans

被引:7
|
作者
Ren, Lu [1 ]
Luo, Juan [1 ]
Tan, Linbo [1 ]
Tang, Qiang [1 ]
机构
[1] Chongqing Med Univ, Ctr Lab Teaching & Management, Coll Pharm, Chongqing 400016, Peoples R China
来源
JOURNAL OF ORGANIC CHEMISTRY | 2022年 / 87卷 / 05期
关键词
ALPHA; BETA-UNSATURATED CARBONYL-COMPOUNDS; ONE-POT; ENOL ETHERS; KETONES; ACID; TETRACHLORIDE; DERIVATIVES; ACCESS; CYCLOISOMERIZATION; HYDROAMINATION;
D O I
10.1021/acs.joc.1c02894
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Titanium enolates, in situ-generated from readily available ketones and titanium tetraisopropoxide, undergo domino cross-coupling/cyclodehydration or domino Aldol-addition/cyclocondensation with alpha-chloroketones to provide synthetically valuable furan derivatives. The domino process tolerates a variety of cyclic and acyclic ketones and chloroketones, producing polysubstituted furans and bi-, tri-, and tetracyclic fused furans.
引用
收藏
页码:3167 / 3176
页数:10
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