Sequential reaction of the tricarbonyl[(h 6 -phenyl) carbamate]chromium complex 3 with chiral amide bases (see 4 and 5) and electrophiles yielded planar chiral ortho-substituted complexes 6 with up to 70% enantiomeric excess (ee) (Scheme 2, Table 1 and2). The enantiomer purity could be increased to
Nucleophilic Catalysis of Reactions of Tricarbonyl(trimethylsilylarene)chromium Complexes with Electrophiles
✍ Scribed by Prof. Dr. Franz Effenberger; Dipl.-Chem. Klaus Schöllkopf
- Publisher
- John Wiley and Sons
- Year
- 1981
- Tongue
- English
- Weight
- 246 KB
- Volume
- 20
- Category
- Article
- ISSN
- 0044-8249
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📜 SIMILAR VOLUMES
7a)["l). The conjugative stabilization accompanying the formation of the pyrromethenic partial structure in the C,Dring region presumably promotes an eventual didehydrogenation step["' to (6). The same partial structure also occurs in the hexahydroporphinoid ligand system (1). The transformation (5
Base hydrolysis reactions of [Cr(tmpa)(NCSe)] 2 O 2ϩ , [Cr(tmpa)(N 3 )] 2 O 2ϩ , and follow the pseudo-first-4ϩ 2ϩ [Cr (tmpa) (ϪO)(ϪPhPO )] [ Cr (tmpa) (ϪO)(ϪCO )] 2 2 4 2 2 3 order relationship (excess OH Ϫ ): For the com- obsd o b p p 3 plex, Ϫ2 Ϫ1 k (60ЊC) ϭ (1.50 Ϯ 0.03) ϫ 10 s ; ⌬H ‡ ϭ 61 Ϯ
Which nucleophiles are capable of attacking the allyl ligand of the Pd-stabilized allyl cation 1? This question is answered by the electrophilicity parameter of 1 which is derived from kinetic investigations.