Ligand-controlled stereodivergent alkenylation of alkynes to access functionalized trans- and cis-1,3-dienes

The stereoselective synthesis of 1,3-dienes represents a challenge in organic synthesis. Here, the authors report a ligand-controlled stereodivergent access to both Z- and E-sulfonyl-1,3-dienes via photoredox and nickel catalysis.

Bibliographic Details
Main Authors: Tianyu Long, Chen Zhu, Ling Li, Liang Shao, Shengqing Zhu, Magnus Rueping, Lingling Chu
Format: Article
Language:English
Published: Nature Portfolio 2023-01-01
Series:Nature Communications
Online Access:https://doi.org/10.1038/s41467-022-35688-2
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author Tianyu Long
Chen Zhu
Ling Li
Liang Shao
Shengqing Zhu
Magnus Rueping
Lingling Chu
author_facet Tianyu Long
Chen Zhu
Ling Li
Liang Shao
Shengqing Zhu
Magnus Rueping
Lingling Chu
author_sort Tianyu Long
collection DOAJ
description The stereoselective synthesis of 1,3-dienes represents a challenge in organic synthesis. Here, the authors report a ligand-controlled stereodivergent access to both Z- and E-sulfonyl-1,3-dienes via photoredox and nickel catalysis.
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spelling doaj.art-02f570f044bf4eea93acb82ca6489f322023-01-08T12:15:23ZengNature PortfolioNature Communications2041-17232023-01-0114111110.1038/s41467-022-35688-2Ligand-controlled stereodivergent alkenylation of alkynes to access functionalized trans- and cis-1,3-dienesTianyu Long0Chen Zhu1Ling Li2Liang Shao3Shengqing Zhu4Magnus Rueping5Lingling Chu6State Key Laboratory for Modification of Chemical Fibers and Polymer Materials, Center for Advanced Low-Dimension Materials, Donghua University, College of Chemistry and Chemical EngineeringKing Abdullah University of Science and Technology (KAUST), KAUST Catalysis Center (KCC)State Key Laboratory for Modification of Chemical Fibers and Polymer Materials, Center for Advanced Low-Dimension Materials, Donghua University, College of Chemistry and Chemical EngineeringState Key Laboratory for Modification of Chemical Fibers and Polymer Materials, Center for Advanced Low-Dimension Materials, Donghua University, College of Chemistry and Chemical EngineeringState Key Laboratory for Modification of Chemical Fibers and Polymer Materials, Center for Advanced Low-Dimension Materials, Donghua University, College of Chemistry and Chemical EngineeringKing Abdullah University of Science and Technology (KAUST), KAUST Catalysis Center (KCC)State Key Laboratory for Modification of Chemical Fibers and Polymer Materials, Center for Advanced Low-Dimension Materials, Donghua University, College of Chemistry and Chemical EngineeringThe stereoselective synthesis of 1,3-dienes represents a challenge in organic synthesis. Here, the authors report a ligand-controlled stereodivergent access to both Z- and E-sulfonyl-1,3-dienes via photoredox and nickel catalysis.https://doi.org/10.1038/s41467-022-35688-2
spellingShingle Tianyu Long
Chen Zhu
Ling Li
Liang Shao
Shengqing Zhu
Magnus Rueping
Lingling Chu
Ligand-controlled stereodivergent alkenylation of alkynes to access functionalized trans- and cis-1,3-dienes
Nature Communications
title Ligand-controlled stereodivergent alkenylation of alkynes to access functionalized trans- and cis-1,3-dienes
title_full Ligand-controlled stereodivergent alkenylation of alkynes to access functionalized trans- and cis-1,3-dienes
title_fullStr Ligand-controlled stereodivergent alkenylation of alkynes to access functionalized trans- and cis-1,3-dienes
title_full_unstemmed Ligand-controlled stereodivergent alkenylation of alkynes to access functionalized trans- and cis-1,3-dienes
title_short Ligand-controlled stereodivergent alkenylation of alkynes to access functionalized trans- and cis-1,3-dienes
title_sort ligand controlled stereodivergent alkenylation of alkynes to access functionalized trans and cis 1 3 dienes
url https://doi.org/10.1038/s41467-022-35688-2
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