Desulfurative Functionalization of β-Acyl Allylic Sulfides with N–H Free Indoles Highly Regioselective at C3 and N1 Positions: Rapid Access to α-Branched Enones-Reference-Cited by-同舟云学术

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Desulfurative Functionalization of β-Acyl Allylic Sulfides with N–H Free Indoles Highly Regioselective at C3 and N1 Positions: Rapid Access to α-Branched Enones

Published:2024-03-19 Issue:7 Volume:89 Page:5200-5206
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Dang Qin-Qin¹,Liu Xue-Ni¹,Li Hui¹,Wen Zhen-Kang¹^ORCID

Affiliation:

1. School of Chemistry and Chemical Engineering, Shanxi University, Taiyuan, Shanxi 030006, China

Funder

Natural Science Foundation for Young Scientists of Shanxi Province

Shanxi University

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.4c00205

Reference72 articles.

1. Transition-metal mediated carbon–sulfur bond activation and transformations

2. Transition-metal mediated carbon–sulfur bond activation and transformations: an update

3. Ni-catalyzed C–S bond construction and cleavage

4. Cleavage of the C(O)–S Bond of Thioesters by Palladium/Norbornene/Copper Cooperative Catalysis: An Efficient Synthesis of 2-(Arylthio)aryl Ketones

5. Selective Ortho Thiolation Enabled by Tuning the Ancillary Ligand in Palladium/Norbornene Catalysis

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