How to Break the Law: trans ‐Hydroboration and gem ‐Hydroboration of Alkynes

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Location: Deutsche Nationalbibliothek Frankfurt am Main

Extent: Online-Ressource

Language: Englisch

Bibliographic citation: How to Break the Law: trans ‐Hydroboration and gem ‐Hydroboration of Alkynes ; day:09 ; month:03 ; year:2023 ; extent:13
Israel journal of chemistry ; (09.03.2023) (gesamt 13)

Creator: Fürstner, Alois

DOI: 10.1002/ijch.202300004

URN: urn:nbn:de:101:1-2023030914395932043286

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

Last update: 14.08.2025, 10:49 AM CEST

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Fürstner, Alois

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Scalable De Novo Synthesis of Aldgarose and Total Synthesis of Aldgamycin N

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Mechanistic Divergence in the Hydrogenative Synthesis of Furans and Butenolides: Ruthenium Carbenes Formed by gem ‐Hydrogenation or through Carbophilic Activation of Alkynes

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How to Break the Law: trans ‐Hydroboration and gem ‐Hydroboration of Alkynes

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Other Objects (12)

Regioselective trans ‐Hydrostannation of Boron‐Capped Alkynes

Mechanistic Divergence in the Hydrogenative Synthesis of Furans and Butenolides: Ruthenium Carbenes Formed by gem ‐Hydrogenation or through Carbophilic Activation of Alkynes

A Sphingolipid Fatty Acid Constituent Made by Alkyne trans ‐Hydrogenation: Total Synthesis of Symbioramide

Modular Synthesis of Furans with up to Four Different Substituents by a trans ‐Carboboration Strategy

Modular Synthesis of Furans with up to Four Different Substituents by a trans ‐Carboboration Strategy

Grubbs Metathesis Enabled by a Light‐Driven gem ‐Hydrogenation of Internal Alkynes

Grubbs Metathesis Enabled by a Light‐Driven gem ‐Hydrogenation of Internal Alkynes

An Efficient and Scalable “Second Generation” Total Synthesis of the Marine Polyketide Limaol Endowed with Antiparasitic Activity

Scalable De Novo Synthesis of Aldgarose and Total Synthesis of Aldgamycin N

Total Synthesis of Mycinamicin IV as Integral Part of a Collective Approach to Macrolide Antibiotics

Light‐Driven gem Hydrogenation: An Orthogonal Entry into “Second‐Generation” Ruthenium Carbene Catalysts for Olefin Metathesis

SYNTHESIS Special Issue in Honor of Professor Sarah Reisman

Regioselective trans ‐Hydrostannation of Boron‐Capped Alkynes

Mechanistic Divergence in the Hydrogenative Synthesis of Furans and Butenolides: Ruthenium Carbenes Formed by gem ‐Hydrogenation or through Carbophilic Activation of Alkynes

A Sphingolipid Fatty Acid Constituent Made by Alkyne trans ‐Hydrogenation: Total Synthesis of Symbioramide

Modular Synthesis of Furans with up to Four Different Substituents by a trans ‐Carboboration Strategy

Modular Synthesis of Furans with up to Four Different Substituents by a trans ‐Carboboration Strategy

Grubbs Metathesis Enabled by a Light‐Driven gem ‐Hydrogenation of Internal Alkynes

Grubbs Metathesis Enabled by a Light‐Driven gem ‐Hydrogenation of Internal Alkynes

An Efficient and Scalable “Second Generation” Total Synthesis of the Marine Polyketide Limaol Endowed with Antiparasitic Activity

Scalable De Novo Synthesis of Aldgarose and Total Synthesis of Aldgamycin N

Total Synthesis of Mycinamicin IV as Integral Part of a Collective Approach to Macrolide Antibiotics

Light‐Driven gem Hydrogenation: An Orthogonal Entry into “Second‐Generation” Ruthenium Carbene Catalysts for Olefin Metathesis

SYNTHESIS Special Issue in Honor of Professor Sarah Reisman

Regioselective trans ‐Hydrostannation of Boron‐Capped Alkynes

Mechanistic Divergence in the Hydrogenative Synthesis of Furans and Butenolides: Ruthenium Carbenes Formed by gem ‐Hydrogenation or through Carbophilic Activation of Alkynes

A Sphingolipid Fatty Acid Constituent Made by Alkyne trans ‐Hydrogenation: Total Synthesis of Symbioramide

Modular Synthesis of Furans with up to Four Different Substituents by a trans ‐Carboboration Strategy

Modular Synthesis of Furans with up to Four Different Substituents by a trans ‐Carboboration Strategy

Grubbs Metathesis Enabled by a Light‐Driven gem ‐Hydrogenation of Internal Alkynes

Grubbs Metathesis Enabled by a Light‐Driven gem ‐Hydrogenation of Internal Alkynes

An Efficient and Scalable “Second Generation” Total Synthesis of the Marine Polyketide Limaol Endowed with Antiparasitic Activity

Scalable De Novo Synthesis of Aldgarose and Total Synthesis of Aldgamycin N

Total Synthesis of Mycinamicin IV as Integral Part of a Collective Approach to Macrolide Antibiotics

Light‐Driven gem Hydrogenation: An Orthogonal Entry into “Second‐Generation” Ruthenium Carbene Catalysts for Olefin Metathesis

SYNTHESIS Special Issue in Honor of Professor Sarah Reisman

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