Ex parte SCHOLL et al. - Page 8




             Appeal No. 1996-2357                                                                                 
             Application 08/124,617                                                                               


             containing any of these species.  We therefore reverse on the                                        
             merits the rejection of claims 4, 7 and 8 over Bögemann, alone                                       
             or with Fujii.                                                                                       
                                Rejections over Boustany or Kleiman,                                              
                                    each alone or in view of Fujii                                                
                    We need only to address claim 3, which is the only                                            
             independent claim.                                                                                   
                    Boustany discloses certain alkyl- and cycloalkyl-nitro-                                       
             benzothiazolyl disulfides as vulcanization accelerators (col.                                        
             1, line 43 - col. 2, line 2).  The benzothiazolyl radical in                                         
             these compounds, unlike that in appellants’ compounds, is                                            
             substituted in the 5 or 6 position with a nitro radical.                                             
             Also, the “R” group in Boustany’s structural formula (col. 1,                                        
             lines 48-56) is alkyl or cycloalkyl and, therefore, differs                                          
             from the polar group to the right of the disulfide linkage in                                        
             the formula in appellants’ claim 3.                                                                  


                    Kleiman discloses a method for making unsymmetrical                                           
             organic disulfides (col. 1, lines 8-16).  The examiner does                                          
             not point to any particular compounds in Kleiman as being                                            
             similar to appellants’ claimed composition.                                                          

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