Bifunctional squaramide-catalyzed synthesis of chiral dihydrocoumarins via ortho-quinone methides generated from 2-(1-tosylalkyl) phenols | |
Gao, Xiang2; Zhou, Yong-Gui2; Zhou, Ji1,2; Wang, Mao-Lin1; Jiang, Guo-Fang1 | |
刊名 | CHEMICAL COMMUNICATIONS |
2017-03-28 | |
卷号 | 53期号:25页码:3531-3534 |
ISSN号 | 1359-7345 |
DOI | 10.1039/c7cc01072a |
文献子类 | Article |
英文摘要 | A bifunctional squaramide-catalyzed reaction of azlactones with o-quinone methides in situ generated from 2-(1-tosylalkyl)-phenols has been successfully developed under basic conditions, providing an efficient and mild access to chiral dihydrocoumarins bearing adjacent tertiary and quaternary stereogenic centers in high yields with excellent diastereo- and enantioselectivities. |
WOS关键词 | DIELS-ALDER REACTION ; ASYMMETRIC-SYNTHESIS ; ENANTIOSELECTIVE SYNTHESIS ; ACTIVATION STRATEGY ; ACID CATALYSIS ; G-QUADRUPLEX ; AZLACTONES ; DERIVATIVES ; QUATERNARY ; ORGANOCATALYSTS |
WOS研究方向 | Chemistry |
语种 | 英语 |
出版者 | ROYAL SOC CHEMISTRY |
WOS记录号 | WOS:000399000100006 |
内容类型 | 期刊论文 |
源URL | [http://cas-ir.dicp.ac.cn/handle/321008/169318] |
专题 | 大连化学物理研究所_中国科学院大连化学物理研究所 |
通讯作者 | Zhou, Yong-Gui; Jiang, Guo-Fang |
作者单位 | 1.Hunan Univ, Coll Chem & Chem Engn, State Key Lab Chemo Biosensing & Chemometr, Changsha 410082, Hunan, Peoples R China 2.Chinese Acad Sci, Dalian Inst Chem Phys, State Key Lab Catalysis, Dalian 116023, Peoples R China |
推荐引用方式 GB/T 7714 | Gao, Xiang,Zhou, Yong-Gui,Zhou, Ji,et al. Bifunctional squaramide-catalyzed synthesis of chiral dihydrocoumarins via ortho-quinone methides generated from 2-(1-tosylalkyl) phenols[J]. CHEMICAL COMMUNICATIONS,2017,53(25):3531-3534. |
APA | Gao, Xiang,Zhou, Yong-Gui,Zhou, Ji,Wang, Mao-Lin,&Jiang, Guo-Fang.(2017).Bifunctional squaramide-catalyzed synthesis of chiral dihydrocoumarins via ortho-quinone methides generated from 2-(1-tosylalkyl) phenols.CHEMICAL COMMUNICATIONS,53(25),3531-3534. |
MLA | Gao, Xiang,et al."Bifunctional squaramide-catalyzed synthesis of chiral dihydrocoumarins via ortho-quinone methides generated from 2-(1-tosylalkyl) phenols".CHEMICAL COMMUNICATIONS 53.25(2017):3531-3534. |
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