Tetrahedron letters

Enhancement of stereoselectivity in catalytic cyclopropanation reactions

MP Doyle, KL Loh, KM DeVries, MS Chinn

Index: Doyle, Michael P.; Loh, Kuo-Liang; DeVries, Keith M.; Chinn, Mitchell S. Tetrahedron Letters, 1987 , vol. 28, # 8 p. 833 - 836

Full Text: HTML

Citation Number: 42

Abstract

Download full text in PDF Opens in a new window. Article suggestions will be shown in a dialog on return to ScienceDirect. ... Please enable JavaScript to use all the features on this page. ... Significant enhancement of trans(anti) stereoselectivity is achieved in rhodium(II) acetamide catalyzed cyclopropanation reactions of 2,3,4-trimethyl-3-pentyl diazoacetate (ODA) and diazoacetamides. ... Highly selective synthesis of trans(anti) cyclopropane derivatives by ...

Related Articles:

Exceptionally high trans (anti) stereoselectivity in catalytic cyclopropanation reactions

[Doyle, Michael P.; Bagheri, Vahid; Wandless, Thomas J.; Harn, Nancy K.; Brinker, David A.; Eagle, Cassandra T.; Loh, Kuo-Liang Journal of the American Chemical Society, 1990 , vol. 112, # 5 p. 1906 - 1912]

Highly selective γ-lactone syntheses by intramolecular carbenoid carbon-hydrogen insertion in rhodium (II) carboxylate and rhodium (II) carboxamide catalyzed …

[Doyle, Michael P.; Bagheri, Vahid; Pearson, Matthew M.; Edwards, John D. Tetrahedron Letters, 1989 , vol. 30, # 50 p. 7001 - 7004]

Highly selective γ-lactone syntheses by intramolecular carbenoid carbon-hydrogen insertion in rhodium (II) carboxylate and rhodium (II) carboxamide catalyzed …

[Doyle, Michael P.; Bagheri, Vahid; Pearson, Matthew M.; Edwards, John D. Tetrahedron Letters, 1989 , vol. 30, # 50 p. 7001 - 7004]

More Articles...