Issue 29, 2008
From the journal:

Chemical Communications

Single-pot triple catalytic transformations based on coupling of in situ generated allyl boronates with in situ hydrolyzed acetals†

Nicklas Selandera  and  Kálmán J. Szabó*a  

* Corresponding authors

a Stockholm University, Arrhenius Laboratory, Department of Organic Chemistry, Stockholm, Sweden
E-mail: kalman@organ.su.se

Abstract

In situ hydrolyzed acetals were coupled with in situ generated allyl boronates in a one-pot procedure, affording regio- and stereodefined homoallyl alcohols, epoxides and amino alcohols.

Graphical abstract: Single-pot triple catalytic transformations based on coupling of in situ generated allyl boronates with in situ hydrolyzed acetals

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Article information

DOI
https://doi.org/10.1039/B804920C
Article type
Communication
Submitted
25 Mar 2008
Accepted
22 Apr 2008
First published
20 May 2008

Chem. Commun., 2008, 3420-3422

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Single-pot triple catalytic transformations based on coupling of in situ generated allyl boronates with in situ hydrolyzed acetals

N. Selander and K. J. Szabó, Chem. Commun., 2008, 3420 DOI: 10.1039/B804920C

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