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  Dimere Oxydationsprodukte aus α-Äthoxy-pyrrol-Derivaten

Bauer, H. (1967). Dimere Oxydationsprodukte aus α-Äthoxy-pyrrol-Derivaten. Chemische Berichte, 100(5), 1701-1703. doi:10.1002/cber.19671000541.

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Item Permalink: https://hdl.handle.net/11858/00-001M-0000-002D-4A0F-4 Version Permalink: https://hdl.handle.net/11858/00-001M-0000-002D-4A10-F
Genre: Journal Article

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ChemBerichte_100_1967_1701.pdf (Any fulltext), 128KB
 
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http://onlinelibrary.wiley.com/doi/10.1002/cber.19671000541/epdf (Any fulltext)
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 Creators:
Bauer, Helmut1, Author           
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1Department of Organic Chemistry, Max Planck Institute for Medical Research, Max Planck Society, ou_1497706              

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 Abstract: 2-Äthoxy-3.4-dimethyl-pyrrol liefert mit PbO2 5.5′-Diäthoxy-3.4.3′-4′-tetramethyl-1.1′-diaza-fulvalen-(2.2′) (2), das durch saure Hydrolyse in 3.4.3′.4′-Tetramethyl-dipyrrochinon (3) übergeführt wird. Aus 2-Äthoxy-indol erhält man mit O2 Indirubin, mit Jod Isoindigo.

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Language(s): deu - German
 Dates: 1966-12-102006-01-211967-05
 Publication Status: Issued
 Pages: 3
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 Rev. Type: Peer
 Identifiers: DOI: 10.1002/cber.19671000541
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Title: Chemische Berichte
  Other : Chem. Ber.
Source Genre: Journal
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Publ. Info: Weinheim : VCH Verlagsgesellschaft mbH
Pages: - Volume / Issue: 100 (5) Sequence Number: - Start / End Page: 1701 - 1703 Identifier: ISSN: 0009-2940
CoNE: https://pure.mpg.de/cone/journals/resource/954926940716