Enantiomerically pure cycloalkenylacetic acid derivatives via Pd-catalyzed asymmetric allylic alkylation and subsequent enantiomeric enrichment via iodolactones-Reference-Cited by-同舟云学术

Enantiomerically pure cycloalkenylacetic acid derivatives via Pd-catalyzed asymmetric allylic alkylation and subsequent enantiomeric enrichment via iodolactones

Published:1994-11 Issue:46 Volume:35 Page:8595-8598
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Sennhenn Peter,Gabler Bert,Helmchen Günter

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference15 articles.

1. Phosphinoaryl- and phosphinoalkyloxazolines as new chiral ligands for enantioselective catalysis: Very high enantioselectivity in palladium catalyzed allylic substitutions

2. Catalysis of allylic substitutions by Pd complexes of oxazolines containing an additional P, S, or Se Center. X-ray crystal structures and solution structures of chiral π-allyl palladium complexes of phosphinoaryloxazolines

3. Enantioselective allylic amination with chiral (phosphino-oxazoline)pd catalysts

4. Chiral Phosphinoaryldihydrooxazoles as Ligands in Asymmetric Catalysis: Pd-Catalyzed Allylic Substitution

5. Asymmetric palladium catalysed allylic substitution using phosphorus containing oxazoline ligands

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