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Volumn 23, Issue 23, 2004, Pages 5459-5470

Asymmetric iridium(I)-catalyzed allylic alkylation of monosubstituted allylic substrates with phosphinooxazolines as ligands. isolation, characterization, and reactivity of chiral (allyl)iridium(III) complexes

Author keywords

[No Author keywords available]

Indexed keywords

CATALYSIS; IRIDIUM COMPOUNDS; ISOMERIZATION; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; REACTION KINETICS; SPECTROSCOPIC ANALYSIS; STOICHIOMETRY; X RAY CRYSTALLOGRAPHY; X RAY DIFFRACTION ANALYSIS;

EID: 9144258517     PISSN: 02767333     EISSN: None     Source Type: Journal    
DOI: 10.1021/om0401105     Document Type: Article
Times cited : (72)

References (73)
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    • The allylic alkylation of alkylallyl acetates (R = Et, i-Pr) has been also studied using the conditions described in Table 1, but only poor yields and selectivities were obtained.
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    • 4], could not yet be unequivocally identified.
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    • Compound 4a has been previously synthesized by following a different procedure and described as a mixture of conformera: Sänchez-Sancho, P.; Mann, E.; Herradön, B. Adv. Synth. Catal. 2001, 343, 360.
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    • Compound 5b was lynthesized by following a procedure illghtly modified from that published.
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    • 2 were unsuccessful, and therefore, a correct elemental analysis of this compound could not be obtained.
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    • Attempts to isolate complex 18 sufficiently pure for elemental analysis were unsuccessful and led to decomposition of the compound.
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