Chemistry: A European Journal 2008-01-01

A gold(I)-catalyzed intramolecular reaction of propargylic/homopropargylic alcohols with oxirane.

Lun-Zhi Dai, Min Shi

Index: Chemistry 14(23) , 7011-8, (2008)

Full Text: HTML

Abstract

The gold(I)-catalyzed cycloisomerization of epoxy alkynes in the presence of a nucleophile is an efficient protocol to provide ketal skeletons with high stereoselectivity. An intramolecular reaction of propargylic/homopropargylic alcohols with oxirane to produce ketal/spiroketals in moderate yields under mild conditions has been reported. Moreover, the mechanism of this kind of reaction has been discussed on the basis of a series of control and (18)O tracer experiments.


Related Compounds

Related Articles:

An integrated microreactor system for self-optimization of a Heck reaction: from micro- to mesoscale flow systems.

2010-09-17

[Angew. Chem. Int. Ed. Engl. 49(39) , 7076-80, (2010)]

Short, enantioselective total synthesis of aflatoxin B2 using an asymmetric [3+2]-cycloaddition step.

2005-08-31

[J. Am. Chem. Soc. 127(34) , 11958-9, (2005)]

Phosphine-catalyzed domino reaction for the synthesis of conjugated 2,3-dihydrofurans from allenoates and Nazarov reagents.

2012-06-01

[Chem. Asian J. 7(7) , 1533-7, (2012)]

First successful application of diphosphite ligands in the asymmetric hydroformylation of dihydrofurans.

2005-03-07

[Chem. Commun. (Camb.) (9) , 1221-3, (2005)]

An efficient carbonyl-alkene metathesis of bicyclic oxetanes: photoinduced electron transfer reduction of the Paternò-Büchi adducts from 2,3-dihydrofuran and aromatic aldehydes.

2006-01-01

[Photochem. Photobiol. Sci. 5(1) , 51-5, (2006)]

More Articles...