Ex parte MILLER et al. - Page 6


                   Appeal No.  2000-0344                                                                                            
                   Application No. 08/718,408                                                                                       

                   productive of the result sought by the applicant.”  In re Gurley,  27 F.3d 551, 553,                             
                   31 USPQ2d 1130, 1131 (Fed. Cir. 1994).                                                                           
                           Here, Neumann teaches oxidative reactions of various substrates with                                     
                   various oxidants, catalyzed by a ruthenium-based catalyst.  Most relevant to the                                 
                   reaction of the instant claims is the oxidation of cyclohexene with t-butyl                                      
                   hydroperoxide, to yield the “en-2-one” product.  See Table 1.  Neumann’s data                                    
                   show that this reaction proceeds with 28.7% yield, with an almost equal                                          
                   percentage (25.2%) of unidentified “other” products.  Neumann concluded that                                     
                   the catalytic system was “highly active” in the presence of t-butyl hydroperoxide,                               
                   but that “selectivity is marred by various nonselective radical reactions leading to                             
                   a large diversity of unidentified products.”  Page 6027, left-hand column.                                       
                           By contrast, Pearson and Muzart teach processes similar to that of the                                   
                   instant claims, but performed with chromium-based catalysts.  Muzart teaches                                     
                   that ? -5 unsaturated steroids were converted to the corresponding ? -5-7-one                                    
                   compound with yields between 40% and 61%.  See the Table on page 4667                                            
                   (runs 1-7).  Muzart characterizes these yields as “fair” (abstract).  Pearson                                    
                   teaches that “the chromium carbonyl-catalysed reaction with the steroidal                                        
                   compounds resulted in very high yields of the 7-oxo derivatives,” specifically 80%                               
                   and 100% yields.  Page 268 (Figure and sentence bridging the columns).                                           
                           Thus, the examiner’s prima facie case depends on whether a person of                                     
                   ordinary skill in the art would have been led to replace a chromium-based                                        
                   catalyst that produced yields of between 40% and 100% of the desired product,                                    
                   with a ruthenium -based catalyst that produced the desired product with a yield of                               


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