Carboxonium‐Ionen‐Reaktionen cyclischer Acetale, VI. Der sterische Verlauf der säurekatalysierten Umlagerung von 4,5‐Dihydro‐1,3‐dioxepinen zu Tetrahydrofuran‐3‐carbaldehyden-Reference-Cited by-同舟云学术

Carboxonium‐Ionen‐Reaktionen cyclischer Acetale, VI. Der sterische Verlauf der säurekatalysierten Umlagerung von 4,5‐Dihydro‐1,3‐dioxepinen zu Tetrahydrofuran‐3‐carbaldehyden

Published:1982-08 Issue:8 Volume:115 Page:2728-2743
ISSN:0009-2940
Container-title:Chemische Berichte
language:en
Short-container-title:Chem. Ber.

Author:

Frauenrath Herbert¹,Runsink Jan¹,Scharf Hans‐Dieter¹

Affiliation:

1. Institut für Organische Chemie der Technischen Hochschule Aachen, Prof.‐Pirlet‐Str. 1, D‐5100 Aachen

Publisher

Wiley

Subject

Inorganic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/cber.19821150806

Reference16 articles.

1. Carboxonium-ionen-reaktionen V. synthese von 1,3-oxathiolen und deren fragmentierung zu β-thia-γ,δ-enonen

2. Fragmentierung cyclischer Carboxonium‐Ionen, III. 1,3‐Dioxepan‐4‐ylium‐Ionen, Schlüssel zur Synthese von Tetrahydrofuran‐3‐carbaldehyden

3. Stereoselective synthesis of tetrahydrofuran-3-carbaldehyde

4. Spezifikation der molekularen Chiralität

5. Specification of Molecular Chirality

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