Premium
A Catalyst‐Free Cycloaddition Reaction: Access to Spiro[chroman‐3,2’‐indene‐1’,3’‐dione] Scaffolds
Author(s) -
Han Yuzhe,
Zhu Yingzu,
Zhang Pangmiaomiao,
Li Wenjun,
Li Pengfei
Publication year - 2017
Publication title -
chemistryselect
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.437
H-Index - 34
ISSN - 2365-6549
DOI - 10.1002/slct.201702398
Subject(s) - indane , diastereomer , cycloaddition , chemistry , indene , catalysis , combinatorial chemistry , organic chemistry , stereochemistry
We have reported herein a catalyst‐free cycloaddition of ortho ‐hydroxyphenyl‐substituted para ‐quinone methides and 2‐arylideneindane‐1,3‐diones by which a series of chromans featuring a spiro indane‐1,3‐dione scaffolds were obtained in high yields without any additives. Importantly, both anti ‐ and syn ‐ diastereomers could be obtained as single diastereomers respectively. Moverover, the current methold provides a novel and convenient approach for the efficient incorporation of the two biologically important scaffolds (chroman and spiro indane‐1,3‐dione).
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom