Chlorodimethylaluminum-promoted nucleophilic addition of lithium pentamethylcyclopentadienide to aliphatic aldehydes and DDQ-mediated carbon–carbon bond cleavage of the adducts providing the parent aldehydes-Reference-Cited by-同舟云学术

Chlorodimethylaluminum-promoted nucleophilic addition of lithium pentamethylcyclopentadienide to aliphatic aldehydes and DDQ-mediated carbon–carbon bond cleavage of the adducts providing the parent aldehydes

Published:2006-01 Issue:2 Volume:47 Page:163-166
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Uemura Minoru,Yorimitsu Hideki,Oshima Koichiro

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference23 articles.

1. Pentamethylcyclopentadienide in organic synthesis: nucleophilic addition of lithium pentamethylcyclopentadienide to aromatic aldehydes and carbon–carbon bond cleavage of the adducts affording the parent aldehydes

2. Communications- Preparation of 1,2,3,4,5-Pentamethyl-cyclopentadiene, 1,2,3,4,5,5-Hexamethyl-cyclopentadiene, and 1,2,3,4,5-Pentamethyl-cyclopentadienylcarbinol

3. Zur Umsetzung von (Pentamethylcyclopentadienyl)lithium mit Halogenmethanen und Formylverbindungen

4. Eine Untersuchung an 6‐Deuterio‐ endo ‐ und‐ exo ‐6‐isopropyl‐1,2,3,5‐tetramethyl‐4‐methylenbicyclo[3.1.0]hex‐2‐en über den Mechanismus der Singulett‐angeregten Photo‐Isomerisierung des Homofulven‐Systems

5. Substituenten‐Einfluß auf die lichtinduzierte Isomerisierung des Homofulven‐Systems: Photo‐Isomerisierung des Singulettangeregten 1,2,3,5‐Tetramethyl‐4‐methylen‐ endo ‐ und‐ exo ‐6‐(trifluormethyl)bicyclo[3.1.0]hex‐2‐ens

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