relation: http://d-scholarship-dev.library.pitt.edu/20483/
title: Water-Accelerated Tandem Claisen Rearrangement-Catalytic Asymmetric Carboalumination
creator: Wipf, P
creator: Ribe, S
description: matrix presented The addition of stoichiometric quantities of water accelerates both the trimethylaluminum-mediated aromatic Claisen reaction and the chiral zirconocene-catalyzed asymmetric carboalumination of terminal alkenes. The two reactions occur in a tandem sequence resulting in the selective formation of two new C-C and one C-O bond after oxidative quench of the intermediate trialkylalane.
date: 2001-05-17
type: Article
type: PeerReviewed
format: text/plain
language: en
rights: attached
identifier: http://d-scholarship-dev.library.pitt.edu/20483/1/licence.txt
identifier:   Wipf, P and Ribe, S  (2001) Water-Accelerated Tandem Claisen Rearrangement-Catalytic Asymmetric Carboalumination.  Organic Letters, 3 (10).  1503 - 1505.  ISSN 1523-7060     
relation: 10.1021/ol015816z