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If I understand the question correctly (I do not have the book), it goes like this: (Ref. J. Am. Chem. Soc. 85, 2, 207-222)

In short I would say that it is not possible to perform the reaction in question in the same way with the Stork enamine alkylation simply because—due to the α,β unsaturation of the ketone—the enamine can not be produced with pyrrolidine. Also, I performed a Reaxys search and found no relevant results. (Of course, I might have missed something.) However, I did find a couple of interesting reactions between cyclohexenone and pyrrolidine which I submit below for completion:

And the following L-Proline organocatalytic reaction taken from: Tetrahedron Letters, 2010, vol. 51, #38, p. 5086 - 5090. Note that compounds 1 and 2 in the scheme were isolated.

However it must be noted that generally, using a different α, β unsaturated ketone and a different amine to the ones used above, the reaction in question is possible as demonstrated by user55119 in his answer here: https://chemistry.stackexchange.com/questions/99987/why-enamine-formation-does-not-occur-with-α-β-unsaturated-ketones?noredirect=1#comment186687_99990

If I understand the question correctly (I do not have the book), it goes like this: (Ref. J. Am. Chem. Soc. 85, 2, 207-222)

In short I would say that it is not possible to perform the reaction in question in the same way with the Stork enamine alkylation simply because—due to the α,β unsaturation of the ketone—the enamine can not be produced with pyrrolidine. Also, I performed a Reaxys search and found no relevant results. (Of course, I might have missed something.) However, I did find a couple of interesting reactions between cyclohexenone and pyrrolidine which I submit below for completion:

And the following L-Proline organocatalytic reaction taken from: Tetrahedron Letters, 2010, vol. 51, #38, p. 5086 - 5090. Note that compounds 1 and 2 in the scheme were isolated.

However it must be noted that generally, using a different α, β unsaturated ketone and a different amine to the ones used above, the reaction in question is possible as demonstrated by user55119 in his answer here: https://chemistry.stackexchange.com/questions/99987/why-enamine-formation-does-not-occur-with-α-β-unsaturated-ketones?noredirect=1#comment186687_99990

If I understand the question correctly (I do not have the book), it goes like this: (Ref. J. Am. Chem. Soc. 85, 2, 207-222)

In short I would say that it is not possible to perform the reaction in question in the same way with the Stork enamine alkylation simply because—due to the α,β unsaturation of the ketone—the enamine can not be produced with pyrrolidine. Also, I performed a Reaxys search and found no relevant results. (Of course, I might have missed something.) However, I did find a couple of interesting reactions between cyclohexenone and pyrrolidine which I submit below for completion:

And the following L-Proline organocatalytic reaction taken from: Tetrahedron Letters, 2010, vol. 51, #38, p. 5086 - 5090. Note that compounds 1 and 2 in the scheme were isolated.

However it must be noted that generally, using a different α, β unsaturated ketone and a different amine to the ones used above, the reaction in question is possible as demonstrated by user55119 in his answer here: https://chemistry.stackexchange.com/questions/99987/why-enamine-formation-does-not-occur-with-α-β-unsaturated-ketones?noredirect=1#comment186687_99990

If I understand the question correctly (I do not have the book), it goes like this: (Ref. J. Am. Chem. Soc. 85, 2, 207-222)

In short I would say that it is not possible to perform the reaction in question in the same way with the Stork enamine alkylation simply because—due to the α,β unsaturation of the ketone—the enamine can not be produced with pyrrolidine. Also, I performed a Reaxys search and found no relevant results. (Of course, I might have missed something.) However, I did find a couple of interesting reactions between cyclohexenone and pyrrolidine which I submit below for completion:

And the following L-Proline organocatalytic reaction taken from: Tetrahedron Letters, 2010, vol. 51, #38, p. 5086 - 5090. Note that compounds 1 and 2 in the scheme were isolated.

However it must be noted that generally, using a different α, β unsaturated ketone and a different amine to the ones used above, the reaction in question is possible as demonstrated by user55119 in his answer here: https://chemistry.stackexchange.com/questions/99987/why-enamine-formation-does-not-occur-with-α-β-unsaturated-ketones?noredirect=1#comment186687_99990

If I understand the question correctly (I do not have the book), it goes like this: (Ref. J. Am. Chem. Soc. 85, 2, 207-222)

In short I would say that it is not possible to perform the reaction in question in the same way with the Stork enamine alkylation simply because—due to the α,β unsaturation of the ketone—the enamine can not be produced. Also, I performed a Reaxys search and found no relevant results. (Of course, I might have missed something.) However, I did find a couple of interesting reactions between cyclohexenone and pyrrolidine which I submit below for completion:

And the following L-Proline organocatalytic reaction taken from: Tetrahedron Letters, 2010, vol. 51, #38, p. 5086 - 5090. Note that compounds 1 and 2 in the scheme were isolated.

If I understand the question correctly (I do not have the book), it goes like this: (Ref. J. Am. Chem. Soc. 85, 2, 207-222)

In short I would say that it is not possible to perform the reaction in question in the same way with the Stork enamine alkylation simply because—due to the α,β unsaturation of the ketone—the enamine can not be produced with pyrrolidine. Also, I performed a Reaxys search and found no relevant results. (Of course, I might have missed something.) However, I did find a couple of interesting reactions between cyclohexenone and pyrrolidine which I submit below for completion:

And the following L-Proline organocatalytic reaction taken from: Tetrahedron Letters, 2010, vol. 51, #38, p. 5086 - 5090. Note that compounds 1 and 2 in the scheme were isolated.

However it must be noted that generally, using a different α, β unsaturated ketone and a different amine to the ones used above, the reaction in question is possible as demonstrated by user55119 in his answer here: https://chemistry.stackexchange.com/questions/99987/why-enamine-formation-does-not-occur-with-α-β-unsaturated-ketones?noredirect=1#comment186687_99990