Silaboration of [1.1.1]Propellane: A Storable Feedstock for Bicyclo[1.1.1]pentane Derivatives-Reference-Cited by-同舟云学术

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Silaboration of [1.1.1]Propellane: A Storable Feedstock for Bicyclo[1.1.1]pentane Derivatives

Published:2020-01-27 Issue:5 Volume:59 Page:1970-1974
ISSN:1433-7851
Container-title:Angewandte Chemie International Edition
language:en
Short-container-title:Angew. Chem. Int. Ed.

Author:

Kondo Masaki¹,Kanazawa Junichiro¹²^ORCID,Ichikawa Tomohiro¹,Shimokawa Takumi¹,Nagashima Yuki¹,Miyamoto Kazunori¹²^ORCID,Uchiyama Masanobu¹²³^ORCID

Affiliation:

1. Graduate School of Pharmaceutical SciencesThe University of Tokyo 7-3-1 Hongo, Bunkyo-ku Tokyo 113-0033 Japan

2. Cluster for Pioneering Research (CPR)Advanced Elements Chemistry LaboratoryRIKEN 2-1 Hirosawa Wako Saitama 351-0198 Japan

3. Research Initiative for Supra-Materials (RISM)Shinshu University 3-15-1 Tokida, Ueda Nagano 386-8567 Japan

Funder

Japan Society for the Promotion of Science

Nagase Science Technology Foundation

Sumitomo Foundation

Publisher

Wiley

Subject

General Chemistry,Catalysis

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/anie.201909655

Reference64 articles.

1.

2. (S)-(+)-2-(3‘-Carboxybicyclo[1.1.1]pentyl)- glycine, a Structurally New Group I Metabotropic Glutamate Receptor Antagonist

3. Application of the Bicyclo[1.1.1]pentane Motif as a Nonclassical Phenyl Ring Bioisostere in the Design of a Potent and Orally Active γ-Secretase Inhibitor

4. Synthesis of Bicyclo[1.1.1]pentane Bioisosteres of Internal Alkynes and para ‐Disubstituted Benzenes from [1.1.1]Propellane

5. Synthese von Bicyclo[1.1.1]pentan‐Bioisosteren von internen Alkinen und para ‐disubstituierten Benzolen unter Verwendung von [1.1.1]Propellan

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1. Light-enabled scalable synthesis of bicyclo[1.1.1]pentane halides and their functionalizations;Nature Synthesis;2024-09-05

2. Uncatalyzed Diboron Activation by a Strained Hydrocarbon: Experimental and Theoretical Study of [1.1.1]Propellane Diborylation;Chemistry – A European Journal;2024-08-30

3. Photoinduced C(sp³)−H Bicyclopentylation Enabled by an Electron Donor–Acceptor Complex‐Mediated Chemoselective Three‐Component Radical Relay;Angewandte Chemie International Edition;2024-08-21

4. Photoinduced C(sp³)−H Bicyclopentylation Enabled by an Electron Donor–Acceptor Complex‐Mediated Chemoselective Three‐Component Radical Relay;Angewandte Chemie;2024-08-21

5. Photoinduced Multicomponent Heteroarylation of [1.1.1]Propellane with Katritzky Pyridinium Salts;Organic Letters;2024-08-14

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