当前位置: X-MOL 学术Angew. Chem. Int. Ed. › 论文详情
Our official English website, www.x-mol.net, welcomes your feedback! (Note: you will need to create a separate account there.)
Catalytic Enantioselective 1,3‐Alkyl Shift in Alkyl Aryl Ethers: Efficient Synthesis of Optically Active 3,3′‐Diaryloxindoles
Angewandte Chemie International Edition ( IF 16.6 ) Pub Date : 2018-04-20 , DOI: 10.1002/anie.201801650
Amol B. Gade 1, 2 , Pradip N. Bagle 1, 2 , Popat S. Shinde 1, 2 , Vipin Bhardwaj 3 , Subhrashis Banerjee 4 , Ajit Chande 3 , Nitin T. Patil 5
Affiliation  

Reported is the first organocatalytic asymmetric 1,3‐alkyl shift in alkyl aryl ethers for the synthesis of chiral 3,3′‐diaryloxindoles using a chiral Brønsted acid catalyst. Preliminary results showed that each enantiomer of the 3,3′‐diaryloxindole, and a racemic mixture, showed different antiproliferative activities against HeLa cell lines by using an MTT assay.

中文翻译:

烷基芳醚中的催化对映选择性1,3-烷基转移:光学活性3,3'-二芳基吲哚的高效合成

报道了使用手性布朗斯台德酸催化剂合成手性3,3'-二芳基吲哚的烷基芳基醚中的第一个有机催化不对称的1,3-烷基转移。初步结果显示,通过使用MTT分析,3,3'-二芳基吲哚的每个对映异构体和外消旋混合物对HeLa细胞系均表现出不同的抗增殖活性。
更新日期:2018-04-20
down
wechat
bug