Synthesis of Tri‐ and Tetrasubstituted Alkenyl Boronates from Alkynes

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Location: Deutsche Nationalbibliothek Frankfurt am Main

Extent: Online-Ressource

Language: Englisch

Bibliographic citation: Synthesis of Tri‐ and Tetrasubstituted Alkenyl Boronates from Alkynes ; volume:2022 ; number:30 ; year:2022 ; extent:21
European journal of organic chemistry ; 2022, Heft 30 (2022) (gesamt 21)

Creator: Altarejos, Julia
Valero, Antonio
Manzano, Rubén
Carreras, Javier

DOI: 10.1002/ejoc.202200521

URN: urn:nbn:de:101:1-2022080915111145416142

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

Last update: 15.08.2025, 7:35 AM CEST

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Altarejos, Julia
Valero, Antonio
Manzano, Rubén
Carreras, Javier

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Further Improvements of the Synthesis of Alkynes from Aldehydes

De Novo Synthesis of Pyridones From Enaminones and Alkynes

Palladium‐Catalyzed Oxidative Synthesis of α‐Acetoxylated Enones from Alkynes

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Copper-mediated synthesis of N-alkenyl-α,β-unsaturated nitrones and their conversion to tri- and tetrasubstituted pyridines

Further Improvements of the Synthesis of Alkynes from Aldehydes

De Novo Synthesis of Pyridones From Enaminones and Alkynes

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Synthesis of Tri‐ and Tetrasubstituted Alkenyl Boronates from Alkynes

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Other Objects (12)

Cobalt-catalyzed hydrothiolation of alkynes for the diverse synthesis of branched alkenyl sulfides

Di- and Tri-substituted Alkenyl Nitriles

Direct Catalytic Synthesis of Ynamides from Alkynes

Ruthenium‐Catalyzed Synthesis of Aryl and Alkenyl Halides from Fluorosulfonates

Lecture 13: Reactions, Synthesis, & Alkynes

Palladium(II)-Catalyzed Redox-Neutral Cyclizations of Alkynes Containing Alkenyl or Electrophilic Functional Groups: A Convenient Synthesis of Carbocycles and Heterocycles

Copper-mediated synthesis of N-alkenyl-α,β-unsaturated nitrones and their conversion to tri- and tetrasubstituted pyridines

Further Improvements of the Synthesis of Alkynes from Aldehydes

De Novo Synthesis of Pyridones From Enaminones and Alkynes

Palladium‐Catalyzed Oxidative Synthesis of α‐Acetoxylated Enones from Alkynes

Palladium‐Catalyzed Oxidative Synthesis of α‐Acetoxylated Enones from Alkynes

Carbolithiation of N-alkenyl ureas and N-alkenyl carbamates

Cobalt-catalyzed hydrothiolation of alkynes for the diverse synthesis of branched alkenyl sulfides

Di- and Tri-substituted Alkenyl Nitriles

Direct Catalytic Synthesis of Ynamides from Alkynes

Ruthenium‐Catalyzed Synthesis of Aryl and Alkenyl Halides from Fluorosulfonates

Lecture 13: Reactions, Synthesis, & Alkynes

Palladium(II)-Catalyzed Redox-Neutral Cyclizations of Alkynes Containing Alkenyl or Electrophilic Functional Groups: A Convenient Synthesis of Carbocycles and Heterocycles

Copper-mediated synthesis of N-alkenyl-α,β-unsaturated nitrones and their conversion to tri- and tetrasubstituted pyridines

Further Improvements of the Synthesis of Alkynes from Aldehydes

De Novo Synthesis of Pyridones From Enaminones and Alkynes

Palladium‐Catalyzed Oxidative Synthesis of α‐Acetoxylated Enones from Alkynes

Palladium‐Catalyzed Oxidative Synthesis of α‐Acetoxylated Enones from Alkynes

Carbolithiation of N-alkenyl ureas and N-alkenyl carbamates

Cobalt-catalyzed hydrothiolation of alkynes for the diverse synthesis of branched alkenyl sulfides

Di- and Tri-substituted Alkenyl Nitriles

Direct Catalytic Synthesis of Ynamides from Alkynes

Ruthenium‐Catalyzed Synthesis of Aryl and Alkenyl Halides from Fluorosulfonates

Lecture 13: Reactions, Synthesis, & Alkynes

Palladium(II)-Catalyzed Redox-Neutral Cyclizations of Alkynes Containing Alkenyl or Electrophilic Functional Groups: A Convenient Synthesis of Carbocycles and Heterocycles

Copper-mediated synthesis of N-alkenyl-α,β-unsaturated nitrones and their conversion to tri- and tetrasubstituted pyridines

Further Improvements of the Synthesis of Alkynes from Aldehydes

De Novo Synthesis of Pyridones From Enaminones and Alkynes

Palladium‐Catalyzed Oxidative Synthesis of α‐Acetoxylated Enones from Alkynes

Palladium‐Catalyzed Oxidative Synthesis of α‐Acetoxylated Enones from Alkynes

Carbolithiation of N-alkenyl ureas and N-alkenyl carbamates

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