1,3-Diethynylbicyclo[1.1.1]pentane, a Useful Molecular Building Block
Author:
Publisher
Wiley
Subject
Organic Chemistry,Physical and Theoretical Chemistry
Reference31 articles.
1. Molecular Rods. 1. Simple Axial Rods
2. Reduction of [1.1.1]propellane with lithium 4,4′-Di-t-butylbiphenyl: Bicyclo[1.1.1]pent-1,3-diyldilithium
3. Das Bicyclo[1.1.1]pentan-Gerüst, ein ausgezeichnetes Relais für π/σ-Konjugation
4. Correlation effects in the long-range coupling between acetylenic π-electrons in a series of α,ω-diethynyl[n]staffanes (n = 1–5)
5. Synthesis and Structure of Trigonal and Tetragonal Connectors for a “Tinkertoy” Construction Set
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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. Definition of the tetrel bond;CrystEngComm;2023
3. Electrochemical test of flexibility of pyridine terminated molecular rods;Electrochimica Acta;2022-07
4. Synthesis and Use of Bicyclo[1.1.1]pentylaldehyde Building Blocks;The Journal of Organic Chemistry;2022-01-20
5. Polyhalogenated Bicyclo[1.1.1]pentane-1,3-dicarboxylic Acids;The Journal of Organic Chemistry;2021-07-16
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