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...

Full description

Bibliographic Details
Main Authors: Xiangfeng Lin, Xianghui Liu, Kai Wang, Qian Li, Yan Liu, Can Li
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