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Allylic derivatives nucleophilic substitution, Tsuji-Trost reaction

The formation of chromane derivatives has also been realised in the palladium catalyzed intramolecular nucleophilic substitution of allyl carbonates (Tsuji-Trost reaction). In most cases the reaction is accompanied by the formation of a new centre of chirality. Using Trost s chiral ligand the ring closure was carried out in an enantioselective manner. The asymmetric allylation of the phenol derivative shown in 4.20. was achieved both in good yield and with excellent selectivity.23... [Pg.75]

The palladium catalyzed intramolecular nucleophilic substitution of allyl alcohol derivatives (Tsuji-Trost reaction) has successfully been extended to the closure of a seven membered ring. The coupling of the allyl alcohol unit and the enamide was the key step in the preparation of the natural product claviciptic acid (5.14.),14... [Pg.92]

Leaving groups in the Tsuji-Trost reaction include acetates, halides, ethers, carbonates, sulfones, carbamates, epoxides, and phosphates. Reviews (a) Tsuji, J. In Handbook of Organopalladium Chemistry for Organic Synthesis, Negishi, E. deMeijere, A., Eds. Wiley-lnterscience New York, 2002 Vol II, Palladium-Catalyzed Nucleophile Substitution Involving Allyl Palladium, Propargyl-palladium and Related Derivatives, pp. 1669-1687. (b) Frost C. G. Howarth, J. Williams, J. M. J. Tetrahedron Asymmetry 1992, 3, 1089-1122. [Pg.170]

One distinguishes palladium(0)- and palladium(ll)-catalysed reactions. The most common palladium(O) transformations are the Mizoroki-Heck and the cross-coupling transformations such as the Suzuki-Miyaura, the Stille and the Sonogashira reactions, which allow the arylation or alkenylation of C=C double bonds, boronic acid derivates, stan-nanes and alkynes respectively [2]. Another important palladium(O) transformation is the nucleophilic substitution of usually allylic acetates or carbonates known as the Tsuji-Trost reaction [3]. The most versatile palladium(ll)-catalysed transformation is the Wacker oxidation, which is industrially used for the synthesis of acetaldehyde from ethylene [4]. It should be noted that many of these palladium-catalysed transformations can also be performed in an enantioselective way [5]. [Pg.282]


See other pages where Allylic derivatives nucleophilic substitution, Tsuji-Trost reaction is mentioned: [Pg.458]    [Pg.217]    [Pg.133]    [Pg.147]    [Pg.186]   


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5-Allyl-derivatives

Allylation Tsuji-Trost reaction

Allylation nucleophiles

Allylation reactions. Tsuji-Trost reaction

Allylic derivatives

Allylic derivatives nucleophilic substitution

Allylic derivatives reactions

Allylic substitution

Allylic substitution nucleophiles

Allylic substitution reactions derivatives

Nucleophiles derivatives

Nucleophiles substitution reactions

Nucleophilic allylic substitution

Nucleophilic reactions allylations

Nucleophilic reactions allylic substitution

Nucleophilic substitution reactions nucleophiles

Substituted derivatives

Substitution reactions allylic

Substitution reactions nucleophile

Substitution reactions nucleophilic

Tsuji

Tsuji allylation

Tsuji-Trost allylic substitution

Tsuji-Trost nucleophilic substitution

Tsuji-Trost reaction nucleophilic substitution

Tsuji-Trost reaction reactions

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