Stereoselective Domino Carbocyclizations of γ- and δ-Cyano-N-tosylhydrazones with Alkenylboronic Acids with Formation of Two Different C(sp3)–C(sp2) Bonds on a Quaternary Stereocenter-Reference-Cited by-同舟云学术

Stereoselective Domino Carbocyclizations of γ- and δ-Cyano-N-tosylhydrazones with Alkenylboronic Acids with Formation of Two Different C(sp3)–C(sp2) Bonds on a Quaternary Stereocenter

Published:2016-09-12 Issue:37 Volume:138 Page:12061-12064
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Plaza Manuel¹,Valdés Carlos¹

Affiliation:

1. Departamento de Química Orgánica e Inorgánica and Instituto Universitario de Química Organometálica “Enrique Moles”, Universidad de Oviedo, c/Julián Clavería 8, 33006 Oviedo, Spain

Funder

Ministerio de Economía y Competitividad

Fundación para el Fomento en Asturias de la Investigación Científica Aplicada y la Tecnología

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/jacs.6b08116

Reference48 articles.

1. Domino Reactions

2. Catalytic Enantioselective Cyclization/Cross-Coupling with Alkyl Electrophiles

3. Recent Advances in Palladium-Catalyzed Cascade Cyclizations

Cited by 53 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Who is Who in the Carbene Chemistry of N‐Sulfonyl Hydrazones;Chinese Journal of Chemistry;2024-05-27

2. Silver-Promoted Rapid Synthesis of 3-Arylindan-1-ones: Microwave-Assisted Reductive Coupling of N-Tosylhydrazone and Boronic Acids;The Journal of Organic Chemistry;2024-05-20

3. Light-induced arylation (alkylation) of N-sulfonylhydrazones with boronic acids;Chemical Communications;2024

4. Homologation of Boronic Acids and Organoboranes by Transition‐Metal‐Free Reactions with Diazo Compounds and N ‐Sulfonylhydrazones;Homologation Reactions;2023-05-26

5. Selective Formal Carbene Insertion into Carbon‐Boron Bonds of Diboronates by N ‐Trisylhydrazones;Angewandte Chemie International Edition;2023-01-24