New Method of Preparation of Brassinosteroids

1994 ◽  
Vol 59 (2) ◽  
pp. 457-460 ◽  
Author(s):  
Ladislav Kohout
Keyword(s):  

Brassinosteroids with lactone B-ring (II and IV) were prepared by oxidation of the corresponding 6-keto derivatives I and III without protection of the hydroxyl groups against the action of the oxidation reagent.

ChemInform ◽  
2010 ◽  
Vol 23 (4) ◽  
pp. no-no
Author(s):  
C. W. HOLZAPFEL ◽  
J. J. HUYSER ◽  
T. L. VAN DER MERWE ◽  
F. R. VAN HEERDEN

Heterocycles ◽  
1991 ◽  
Vol 32 (8) ◽  
pp. 1445 ◽  
Author(s):  
Cedric W. Holzapfel ◽  
Johan J. Huyser ◽  
Thilo L. van der Merwe ◽  
Fanie R. van Heerden

2006 ◽  
Vol 84 (5) ◽  
pp. 812-818 ◽  
Author(s):  
Razieh Fazaeli ◽  
Shahram Tangestaninejad ◽  
Hamid Aliyan

Tosylation of some alcohols and phenols has been directly carried out with p-toluenesulfonyl chloride using heterodoxy acids (H3PW12O40, H3PMo12O40, AlPW12O40, and AlPMo12O40) as catalysts in the absence of solvent. We found that heteropoly acids AlPW12O40 and AlPMo12O40 were effective catalysts for the tosylation of alcohols and phenols. In the case of aliphatic alcohols, secondary alcohols undergo tosylation chemoselectively in the presence of primary hydroxyl groups. This new method consistently has the advantage of excellent yields and short reaction time.Key words: tosylation, p-TsCl, Keggin-type polyoxometalate, solvent-free reaction.


1976 ◽  
Vol 54 (20) ◽  
pp. 3310-3311 ◽  
Author(s):  
Francis C. M. Chen ◽  
N. Leo Benoiton

Methyl iodide and potassium bicarbonate in methanol is presented as a mild, efficient, and selective reagent for the quaternization of amino groups. It does not attack hydroxyl groups. Its use with amino acids, derivatives of lysine, and small peptides is described.


1977 ◽  
Vol 8 (2) ◽  
pp. no-no
Author(s):  
S. CZERNECKI ◽  
C. GEORGOULIS ◽  
C. PROVELENGHIOU
Keyword(s):  

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