Synthesis of Functionalized Cyclooctynes as Building Blocks for Non‐covalent Surface‐Orthogonal Chemistry

Abstract Cyclooctynes substituted with functional groups capable for hydrogen bonding (amide, imide, carboxylic acid) have been synthesized. The 8‐membered ring was derived from cyclooctadiene, by Beckmann rearrangement or by ring‐closing metathesis. The transannular instability of a monocyclic cyclooctyne lactam was postulated. Three stable functionalized cyclooctynes obtained are candidates for a surface‐orthogonal layer‐by‐layer synthesis on semiconductor surfaces (in particular the Si(001) surface).

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Publication Details

Journal
European Journal of Organic Chemistry
Published
2025-03-11
DOI
https://doi.org/10.1002/ejoc.202500124
Citations
1
Primary Topic
Chemical Synthesis and Analysis
Type
article
Field-Weighted Citation Impact
0.81
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article

Synthesis of Functionalized Cyclooctynes as Building Blocks for Non‐covalent Surface‐Orthogonal Chemistry

Ulrich Koert, Dominik Scharf, Sergei I. Ivlev, Clara M. Jaschke
1 citations
European Journal of Organic Chemistry
Chemical Synthesis and Analysis
0.81
article

Synthesis of Functionalized Cyclooctynes as Building Blocks for Non‐covalent Surface‐Orthogonal Chemistry

Ulrich Koert, Dominik Scharf, Sergei I. Ivlev, Clara M. Jaschke
article en
1 citations

Abstract

Abstract Cyclooctynes substituted with functional groups capable for hydrogen bonding (amide, imide, carboxylic acid) have been synthesized. The 8‐membered ring was derived from cyclooctadiene, by Beckmann rearrangement or by ring‐closing metathesis. The transannular instability of a monocyclic cyclooctyne lactam was postulated. Three stable functionalized cyclooctynes obtained are candidates for a surface‐orthogonal layer‐by‐layer synthesis on semiconductor surfaces (in particular the Si(001) surface).

European Journal of Organic ChemistryVol. 28(18)
Philipps University of Marburg (DE)
Openalex Percentile: Top 30%
Chemical Synthesis and Analysis
0.81
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