| title: |
| Domino Twofold Heck / 6p-Electrocyclization and Regioselective Palladium(0)-Catalyzed
Reactions of Brominated Indoles, Furans, Naphthoquinone and 2,4,5,6-Tetrachloropyrimidine |
|
| contributing persons: |
| Munawar Hussain[VerfasserIn] |
 |
143545175 |
| Peter Langer
, Prof. Dr.[AkademischeR BetreuerIn] |
| Scott Taylor
, Prof. Dr.[AkademischeR BetreuerIn] |
| Willi Kantlehner
, Prof. Dr.[AkademischeR BetreuerIn] |
|
| contributing corporate bodies: |
| Universität Rostock, Mathematisch-Naturwissenschaftliche Fakultät[Grad-verleihende Institution] |
|
2147083-2 |
|
| |
| abstract: |
|
I have synthesized functionalized carbazoles and benzofurans based on domino twofold
Heck / 6pi-electrocyclization reactions. Functionalized anthraquinones, fluorenones
and benzocoumarines were also prepared by this methodology. Regioselctive Suzuki-Miyaura
cross-coupling reactions of 2,4,5,6-tetrachloropyrimidine and 2,3,4,5-tetrabromofuran
provided an expedient synthesis of mono-, di-, tri- and tetraaryl-pyrimidines and
di- and tetraarylfurans.
[English] |
|
| document type: |
|
| institution: |
| Faculty of Mathematics and Natural Sciences |
|
| language: |
|
| subject class (DDC): |
| 540 Chemistry & allied sciences |
|
| |
publication /
production: |
Rostock
|
Rostock: Universität Rostock
|
|
2010
|
|
| |
| 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_0000000594 |
| created / modified: |
25.01.2011 / 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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