ChemInform Abstract: A Stereoselective Total Synthesis of (.+-.)-Oppositol by a Doubly Diastereoselective Intramolecular Ester Enolate Alkylation.

ChemInform ◽  
2010 ◽  
Vol 28 (20) ◽  
pp. no-no
Author(s):  
D. KIM ◽  
I. H. KIM
Keyword(s):  
Total Synthesis ◽  
Enolate Alkylation ◽  
Ester Enolate

A total synthesis of (−)-reiswigin a via sequential claisen rearrangement-intramolecular ester enolate alkylation

1994 ◽  
Vol 35 (43) ◽  
pp. 7957-7960 ◽  
Author(s):  
Deukjoon Kim ◽  
Kye Jung Shin ◽  
Ik Yoen Kim ◽  
Sang Woo Park
Keyword(s):  
Total Synthesis ◽  
Claisen Rearrangement ◽  
Enolate Alkylation ◽  
Ester Enolate

A stereoselective synthesis of (±)-elemol via an intramolecular SN2′ ester enolate alkylation

1993 ◽  
Vol 34 (41) ◽  
pp. 6557-6558 ◽  
Author(s):  
Deukjoon Kim ◽  
Joong In Lim ◽  
Kye Jung Shin ◽  
Hak Sung Kim
Keyword(s):  
Stereoselective Synthesis ◽  
Enolate Alkylation ◽  
Ester Enolate
Sign in / Sign up

Export Citation Format

Share Document