Biomimetic approach to the catalytic enantioselective synthesis of tetracyclic isochroman
General and stereoselective synthesis of tetracyclic isochroman-containing polyketide oligomers is challenging. Here, the authors report on an Au(I)/chiral Sc(III) bimetallic catalyst for a biomimetic asymmetric hetero-Diels–Alder reaction for in-situ generation of isochromene and ortho-quinonemethi...
Main Authors: | , , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Nature Publishing Group
2021-08-01
|
Series: | Nature Communications |
Online Access: | https://doi.org/10.1038/s41467-021-25198-y |
id |
doaj-d8067b9568c34fa380fcc342497aa73e |
---|---|
record_format |
Article |
spelling |
doaj-d8067b9568c34fa380fcc342497aa73e2021-08-22T11:40:27ZengNature Publishing GroupNature Communications2041-17232021-08-011211910.1038/s41467-021-25198-yBiomimetic approach to the catalytic enantioselective synthesis of tetracyclic isochromanXiangfeng Lin0Xianghui Liu1Kai Wang2Qian Li3Yan Liu4Can Li5State Key Laboratory of Catalysis, Dalian Institute of Chemical Physics, Chinese Academy of SciencesState Key Laboratory of Catalysis, Dalian Institute of Chemical Physics, Chinese Academy of SciencesState Key Laboratory of Catalysis, Dalian Institute of Chemical Physics, Chinese Academy of SciencesState Key Laboratory of Catalysis, Dalian Institute of Chemical Physics, Chinese Academy of SciencesState Key Laboratory of Catalysis, Dalian Institute of Chemical Physics, Chinese Academy of SciencesState Key Laboratory of Catalysis, Dalian Institute of Chemical Physics, Chinese Academy of SciencesGeneral and stereoselective synthesis of tetracyclic isochroman-containing polyketide oligomers is challenging. Here, the authors report on an Au(I)/chiral Sc(III) bimetallic catalyst for a biomimetic asymmetric hetero-Diels–Alder reaction for in-situ generation of isochromene and ortho-quinonemethide.https://doi.org/10.1038/s41467-021-25198-y |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Xiangfeng Lin Xianghui Liu Kai Wang Qian Li Yan Liu Can Li |
spellingShingle |
Xiangfeng Lin Xianghui Liu Kai Wang Qian Li Yan Liu Can Li Biomimetic approach to the catalytic enantioselective synthesis of tetracyclic isochroman Nature Communications |
author_facet |
Xiangfeng Lin Xianghui Liu Kai Wang Qian Li Yan Liu Can Li |
author_sort |
Xiangfeng Lin |
title |
Biomimetic approach to the catalytic enantioselective synthesis of tetracyclic isochroman |
title_short |
Biomimetic approach to the catalytic enantioselective synthesis of tetracyclic isochroman |
title_full |
Biomimetic approach to the catalytic enantioselective synthesis of tetracyclic isochroman |
title_fullStr |
Biomimetic approach to the catalytic enantioselective synthesis of tetracyclic isochroman |
title_full_unstemmed |
Biomimetic approach to the catalytic enantioselective synthesis of tetracyclic isochroman |
title_sort |
biomimetic approach to the catalytic enantioselective synthesis of tetracyclic isochroman |
publisher |
Nature Publishing Group |
series |
Nature Communications |
issn |
2041-1723 |
publishDate |
2021-08-01 |
description |
General and stereoselective synthesis of tetracyclic isochroman-containing polyketide oligomers is challenging. Here, the authors report on an Au(I)/chiral Sc(III) bimetallic catalyst for a biomimetic asymmetric hetero-Diels–Alder reaction for in-situ generation of isochromene and ortho-quinonemethide. |
url |
https://doi.org/10.1038/s41467-021-25198-y |
work_keys_str_mv |
AT xiangfenglin biomimeticapproachtothecatalyticenantioselectivesynthesisoftetracyclicisochroman AT xianghuiliu biomimeticapproachtothecatalyticenantioselectivesynthesisoftetracyclicisochroman AT kaiwang biomimeticapproachtothecatalyticenantioselectivesynthesisoftetracyclicisochroman AT qianli biomimeticapproachtothecatalyticenantioselectivesynthesisoftetracyclicisochroman AT yanliu biomimeticapproachtothecatalyticenantioselectivesynthesisoftetracyclicisochroman AT canli biomimeticapproachtothecatalyticenantioselectivesynthesisoftetracyclicisochroman |
_version_ |
1721199478204006400 |