Enantioselective desymmetrisation of prochiral four membered carbocycles

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Location: Deutsche Nationalbibliothek Frankfurt am Main

Extent: Online-Ressource

Language: Englisch

Notes: Mainz, Johannes Gutenberg-Universität Mainz, Dissertation, 2023

Keyword: Asymmetrische Synthese
Asymmetrische Reaktion
Chemische Synthese
Chirale Verbindungen
Katalysator

Event: Veröffentlichung

(where): Mainz

(who): Universitätsbibliothek der Johannes Gutenberg-Universität Mainz

(when): 2023

Creator: Tenberge, Marius

DOI: 10.25358/openscience-9361

URN: urn:nbn:de:hebis:77-openscience-0b97c9fc-c50c-4bd7-b9f0-1544118996e89

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

Last update: 15.08.2025, 7:22 AM CEST

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Associated

Tenberge, Marius
Universitätsbibliothek der Johannes Gutenberg-Universität Mainz

Time of origin

2023

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Enantioselective desymmetrisation of prochiral four membered carbocycles

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Other Objects (12)

Formation of an Unusual Four-Membered Nitrogen Ring

Highly strained four-membered heterometallacycles of group 4 metallocenes

Highly strained four-membered heterometallacycles of group 4 metallocenes

Nitrene‐Mediated C−H Oxygenation: Catalytic Enantioselective Formation of Five‐Membered Cyclic Organic Carbonates

Nitrene‐Mediated C−H Oxygenation: Catalytic Enantioselective Formation of Five‐Membered Cyclic Organic Carbonates

Uncommon Four‐Membered Building Blocks – Cyclobutenes, Azetines and Thietes

Enantioselective synthesis of saddle-shaped eight-membered lactones with inherent chirality via organocatalytic high-order annulation

On-Surface Cyclization of ortho-Dihalotetracenes to Four- and Six-Membered Rings

A Neutral Three‐Membered 2π Aromatic Disilaborirane and the Unique Conversion into a Four‐Membered BSi 2 N‐Ring

A Neutral Three‐Membered 2π Aromatic Disilaborirane and the Unique Conversion into a Four‐Membered BSi 2 N‐Ring

Three-membered rings

Investigations on Novel 1,3‐Diazetidine Based Four‐Membered N‐Heterocyclic Carbenes

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Highly strained four-membered heterometallacycles of group 4 metallocenes

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Nitrene‐Mediated C−H Oxygenation: Catalytic Enantioselective Formation of Five‐Membered Cyclic Organic Carbonates

Nitrene‐Mediated C−H Oxygenation: Catalytic Enantioselective Formation of Five‐Membered Cyclic Organic Carbonates

Uncommon Four‐Membered Building Blocks – Cyclobutenes, Azetines and Thietes

Enantioselective synthesis of saddle-shaped eight-membered lactones with inherent chirality via organocatalytic high-order annulation

On-Surface Cyclization of ortho-Dihalotetracenes to Four- and Six-Membered Rings

A Neutral Three‐Membered 2π Aromatic Disilaborirane and the Unique Conversion into a Four‐Membered BSi 2 N‐Ring

A Neutral Three‐Membered 2π Aromatic Disilaborirane and the Unique Conversion into a Four‐Membered BSi 2 N‐Ring

Three-membered rings

Investigations on Novel 1,3‐Diazetidine Based Four‐Membered N‐Heterocyclic Carbenes

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On-Surface Cyclization of ortho-Dihalotetracenes to Four- and Six-Membered Rings

A Neutral Three‐Membered 2π Aromatic Disilaborirane and the Unique Conversion into a Four‐Membered BSi 2 N‐Ring

A Neutral Three‐Membered 2π Aromatic Disilaborirane and the Unique Conversion into a Four‐Membered BSi 2 N‐Ring

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Investigations on Novel 1,3‐Diazetidine Based Four‐Membered N‐Heterocyclic Carbenes

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