Switch from Palladium‐Catalyzed Cycloisomerization/Dimerization of Terminal Allenyl Ketones to Preferential Formation of Monomers by a 5‐Palladatricyclo[4.1.0.0 2,4 ]heptane Catalyst: Synthesis of Furans from Substrates Incompatible with the Commonly Used Silver Catalysts-Reference-Cited by-同舟云学术

Switch from Palladium‐Catalyzed Cycloisomerization/Dimerization of Terminal Allenyl Ketones to Preferential Formation of Monomers by a 5‐Palladatricyclo[4.1.0.0 2,4 ]heptane Catalyst: Synthesis of Furans from Substrates Incompatible with the Commonly Used Silver Catalysts

Published:1997-10 Issue:10 Volume:130 Page:1449-1456
ISSN:0009-2940
Container-title:Chemische Berichte
language:en
Short-container-title:Chem. Ber.

Author:

Hashmi A. Stephen K.¹,Sehwarz Lothar¹

Affiliation:

1. Institut für Organische Chemie der Johann Wolfgang Goethe‐Universität, Marie‐Curie‐Straβe 11, D‐60439 Frankfurt am Main, Germany Fax: (internat.)+ 49(0)69/798‐29464

Publisher

Wiley

Subject

Inorganic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/cber.19971301015

Reference59 articles.

1. A mild method for the synthesis of furans. Application to 2,5-bridged furano macrocyclic compounds

2. Synthesis of furans by silver(I)-promoted cyclization of allenyl ketones and aldehydes

3. Synthesis of 2,5-furanocycles through intraannular cyclization of macrocyclic allenones

4. Observations Regarding the Ag(I)-Catalyzed Conversion of Allenones to Furans

5. Total Synthesis of the Pseudopterane (.+-.)-Kallolide B

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