Stereoselective Synthesis of β-Lactam-triflones under Catalyst-Free Conditions-Reference-Cited by-同舟云学术

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Stereoselective Synthesis of β-Lactam-triflones under Catalyst-Free Conditions

Published:2015-11-09 Issue:22 Volume:17 Page:5610-5613
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Huang Zhongyan¹,Wang Chen¹,Tokunaga Etsuko¹,Sumii Yuji¹,Shibata Norio¹

Affiliation:

1. Department of Nanopharmaceutical Sciences, Nagoya Institute of Technology, Gokiso, Showa-ku, Nagoya 466-8555, Japan

Funder

Kobayashi International Foundation

Japan Agency for Medical Research and Development

Ministry of Education, Culture, Sports, Science, and Technology

Japan Science and Technology Agency

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.5b02827

Reference89 articles.

1. Modern Fluoroorganic Chemistry

2. Organofluorine Compounds

3. Organofluorine Chemistry

4. Understanding organofluorine chemistry. An introduction to the C–F bond

5. Fluorine in Pharmaceutical Industry: Fluorine-Containing Drugs Introduced to the Market in the Last Decade (2001–2011)

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1. Access to Spiro Bis-β-lactams via a Metal-Free Microwave-Assisted Wolff Rearrangement/Staudinger [2+2] Cycloaddition Cascade Involving 3-Diazotetramic Acids and Imines;The Journal of Organic Chemistry;2024-02-16

2. Photocatalyzed sulfoximination/amidation of (Het)arylethenes tethered N-tosyl amide: a versatile entry to sulfoximidoyl β- and γ-lactams;Organic Chemistry Frontiers;2024

3. Preparation and Reactivity Study of a Versatile Trifluoromethylthiolating Agent: S‐Trifluoromethyl Trifluoromethanesulfonothioate (TTST);Angewandte Chemie International Edition;2023-06-28

4. Preparation and Reactivity Study of a Versatile Trifluoromethylthiolating Agent: S‐Trifluoromethyl Trifluoromethanesulfonothioate (TTST);Angewandte Chemie;2023-06-28

5. Catalytic Enantioselective Entry to Triflones Featuring a Quaternary Stereocenter;Organic Letters;2022-06-10

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