| title: |
| Regioselective Synthesis of Functionalized Salicylates, Isotetronic Acids, and Alkylidene-Isobenzofurans
based on One-Pot Cyclizations of Silyl Enol Ethers |
|
| contributing persons: |
| Rüdiger Dede[VerfasserIn] |
 |
135976227 |
| Peter Langer
, Prof. Dr.[AkademischeR BetreuerIn] |
| Peter Langer
, Prof. Dr.[AkademischeR BetreuerIn] |
| Jens Christoffers
, Prof. Dr.[AkademischeR BetreuerIn] |
|
| contributing corporate bodies: |
| Universität Rostock, Mathematisch-Naturwissenschaftliche Fakultät[Grad-verleihende Institution] |
|
2147083-2 |
|
| |
| abstract: |
|
Diese Arbeit ist ein Beitrag zur Chemie verschiedener Silyl-Enol-Ether, die zur regioselektiven
Synthese von funktionalisierten Salicylaten, Isotetronsäuren und Alkyliden-Isobenzofuranen
verwendet wurden.
Zusätzlich wurde die Konkurrenz zwischen der kürzlich entwickelten Domino „Staudinger
/ semi-aza-Wittig / Fragmentierungsreaktion” von γ-Azido-β-hydroxyketonen und der
normalen Aza-Wittig-Reaktion untersucht.
[German] |
|
This work is a contribution to the chemistry of different types of silyl enol ethers
which were applied to the regioselective synthesis of functionalized salicylates,
isotetronic acids, and alkylidene-isobenzofurans.
In addition, the competition between the recently developed domino “Staudinger / semi-aza-Wittig
/ fragmentation” reaction of γ-azido-β-hydroxyketones and the normal aza-Wittig reaction
pathway was studied.
[English] |
|
| document type: |
|
| institution: |
| Faculty of Mathematics and Natural Sciences |
|
| language: |
|
| subject class (DDC): |
| 540 Chemistry & allied sciences |
|
| |
publication /
production: |
Rostock
|
Rostock: Universität Rostock
|
|
2008
|
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| |
| identifiers: |
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| |
| access condition: |
|
| license/rights statement: |
all rights reserved
This work may only be used under the terms of the German Copyright Law (Urheberrechtsgesetz). |
|
|
| RosDok id: |
rosdok_disshab_0000000073 |
| created / modified: |
22.07.2008 / 08.08.2023
|
| metadata license: |
The metadata of this document was dedicated to the public domain
(CC0 1.0 Universal Public Domain Dedication). |
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