scholarly journals Diastereoselective Synthesis of Optically Active C2-Substituted Spiro(4.5)decanes: Two Key Intermediates for Spirovetivane Sesquiterpenes.

1997 ◽  
Vol 45 (3) ◽  
pp. 459-463 ◽  
Author(s):  
Yoshiji TAKEMOTO ◽  
Taiichi OHRA ◽  
Yasuhiro YONETOKU ◽  
Chuzo IWATA
2012 ◽  
Vol 9 (2) ◽  
pp. 81-88 ◽  
Author(s):  
Ervin Kovacs ◽  
Ferenc Farkas ◽  
Angelika Thurner ◽  
Aron Szollosy ◽  
Ferenc Faigl

1998 ◽  
Vol 76 (10) ◽  
pp. 1338-1343 ◽  
Author(s):  
Viviana L Ponzo ◽  
Teodoro S Kaufman

The synthesis of optically active α-alkoxymethyl benzyl alcohols by reaction of polysubstituted benzaldehydes with chiral α-alkoxymethyllithiums, easily obtained by transmetallation of the corresponding α-alkoxystannanes with n-butyllithium, is reported. Chemical yields of the transformation are good while low asymmetric induction (<1.6:1) is obtained. Key words: diastereoselective synthesis, monoprotected glycols, chiral alkoxymethyllithiums, addition to aldehydes, optically active alcohols.


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