Syntheses of 6,7‐Benzotropolone by Using Ring‐Closing Metathesis Variants Obviating a Strongly Acidic Hydrolysis Thereafter

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Location: Deutsche Nationalbibliothek Frankfurt am Main

Extent: Online-Ressource

Language: Englisch

Bibliographic citation: Syntheses of 6,7‐Benzotropolone by Using Ring‐Closing Metathesis Variants Obviating a Strongly Acidic Hydrolysis Thereafter ; day:25 ; month:02 ; year:2022 ; extent:1
European journal of organic chemistry ; (25.02.2022) (gesamt 1)

Creator: Koblischek, Philip
Brückner, Reinhard

DOI: 10.1002/ejoc.202101070

URN: urn:nbn:de:101:1-2022022614053797848931

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 15.08.2025, 7:28 AM CEST

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Koblischek, Philip
Brückner, Reinhard

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Syntheses of 6,7‐benzotropolone by using ring‐closing metathesis variants obviating a strongly acidic hydrolysis thereafter

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Cyclopeptide Synthesis by Ring-Closing Metathesis

Syntheses of 9‐Vinylated Benzotropolones by a Sequence of Acylation, Ring‐Closing Enyne Metathesis, and Oxidation

Syntheses of 9‐vinylated benzotropolones by a sequence of acylation, ring‐closing enyne metathesis, and oxidation

Highly Substrate‐Selective Macrocyclic Ring Closing Metathesis

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Application of olefin cross metathesis in natural product syntheses

Selective Cross‐Metathesis Versus Ring‐Closing Metathesis of Terpenes, Taking the Path Less Travelled

Synthesis of Berkeleylactone A by Ring‐Closing Alkyne Metathesis

Synthesis of Bioactive Macrocycles Involving Ring-Closing Metathesis Strategy

SPS of Seragamide A via Relay-Ring-Closing Metathesis

Syntheses of 6,7‐benzotropolone by using ring‐closing metathesis variants obviating a strongly acidic hydrolysis thereafter

zweidimensionales bewegtes Bild

Olefin metathesis – ring-closing reaction

Cyclopeptide Synthesis by Ring-Closing Metathesis

Syntheses of 9‐Vinylated Benzotropolones by a Sequence of Acylation, Ring‐Closing Enyne Metathesis, and Oxidation

Syntheses of 9‐vinylated benzotropolones by a sequence of acylation, ring‐closing enyne metathesis, and oxidation

Highly Substrate‐Selective Macrocyclic Ring Closing Metathesis

Hochschulschrift

Application of olefin cross metathesis in natural product syntheses

Selective Cross‐Metathesis Versus Ring‐Closing Metathesis of Terpenes, Taking the Path Less Travelled

Synthesis of Berkeleylactone A by Ring‐Closing Alkyne Metathesis

Synthesis of Bioactive Macrocycles Involving Ring-Closing Metathesis Strategy

SPS of Seragamide A via Relay-Ring-Closing Metathesis

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Syntheses of 6,7‐Benzotropolone by Using Ring‐Closing Metathesis Variants Obviating a Strongly Acidic Hydrolysis Thereafter

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Other Objects (12)

Syntheses of 6,7‐benzotropolone by using ring‐closing metathesis variants obviating a strongly acidic hydrolysis thereafter

Olefin metathesis – ring-closing reaction

Cyclopeptide Synthesis by Ring-Closing Metathesis

Syntheses of 9‐Vinylated Benzotropolones by a Sequence of Acylation, Ring‐Closing Enyne Metathesis, and Oxidation

Syntheses of 9‐vinylated benzotropolones by a sequence of acylation, ring‐closing enyne metathesis, and oxidation

Highly Substrate‐Selective Macrocyclic Ring Closing Metathesis

Application of olefin cross metathesis in natural product syntheses

Selective Cross‐Metathesis Versus Ring‐Closing Metathesis of Terpenes, Taking the Path Less Travelled

Selective Cross‐Metathesis Versus Ring‐Closing Metathesis of Terpenes, Taking the Path Less Travelled

Synthesis of Berkeleylactone A by Ring‐Closing Alkyne Metathesis

Synthesis of Bioactive Macrocycles Involving Ring-Closing Metathesis Strategy

SPS of Seragamide A via Relay-Ring-Closing Metathesis

Syntheses of 6,7‐benzotropolone by using ring‐closing metathesis variants obviating a strongly acidic hydrolysis thereafter

Olefin metathesis – ring-closing reaction

Cyclopeptide Synthesis by Ring-Closing Metathesis

Syntheses of 9‐Vinylated Benzotropolones by a Sequence of Acylation, Ring‐Closing Enyne Metathesis, and Oxidation

Syntheses of 9‐vinylated benzotropolones by a sequence of acylation, ring‐closing enyne metathesis, and oxidation

Highly Substrate‐Selective Macrocyclic Ring Closing Metathesis

Application of olefin cross metathesis in natural product syntheses

Selective Cross‐Metathesis Versus Ring‐Closing Metathesis of Terpenes, Taking the Path Less Travelled

Selective Cross‐Metathesis Versus Ring‐Closing Metathesis of Terpenes, Taking the Path Less Travelled

Synthesis of Berkeleylactone A by Ring‐Closing Alkyne Metathesis

Synthesis of Bioactive Macrocycles Involving Ring-Closing Metathesis Strategy

SPS of Seragamide A via Relay-Ring-Closing Metathesis

Syntheses of 6,7‐benzotropolone by using ring‐closing metathesis variants obviating a strongly acidic hydrolysis thereafter

Olefin metathesis – ring-closing reaction

Cyclopeptide Synthesis by Ring-Closing Metathesis

Syntheses of 9‐Vinylated Benzotropolones by a Sequence of Acylation, Ring‐Closing Enyne Metathesis, and Oxidation

Syntheses of 9‐vinylated benzotropolones by a sequence of acylation, ring‐closing enyne metathesis, and oxidation

Highly Substrate‐Selective Macrocyclic Ring Closing Metathesis

Application of olefin cross metathesis in natural product syntheses

Selective Cross‐Metathesis Versus Ring‐Closing Metathesis of Terpenes, Taking the Path Less Travelled

Selective Cross‐Metathesis Versus Ring‐Closing Metathesis of Terpenes, Taking the Path Less Travelled

Synthesis of Berkeleylactone A by Ring‐Closing Alkyne Metathesis

Synthesis of Bioactive Macrocycles Involving Ring-Closing Metathesis Strategy

SPS of Seragamide A via Relay-Ring-Closing Metathesis

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