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Volumn 64, Issue 12, 1999, Pages 4445-4451

C2-symmetric bisphosphinobioxazoline as a chiral ligand. Highly enantioselective palladium-catalyzed allylic substitutions and formation of P,N,N,P tetradentate palladium (II) complexes

Author keywords

[No Author keywords available]

Indexed keywords

ACETIC ACID DERIVATIVE; BISPHOSPHINOBIOXAZOLINE; CYCLOPENTENE DERIVATIVE; LIGAND; MALONIC ACID DERIVATIVE; METHYLAMINE; OXAZOLINE DERIVATIVE; PALLADIUM COMPLEX; UNCLASSIFIED DRUG;

EID: 0345120713     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo990126i     Document Type: Article
Times cited : (52)

References (86)
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    • Significant dialkylation (32%) was occurred using (S)-BINAPO (38% yield, 57% ee of 13). See (a) Trost, B. M.; Murphy, D. J. Organometallics 1985, 4, 1143. (b) Mori, M.; Nukui, S.; Shibasaki, M. Chem. Lett. 1991, 1791. (c) For desymmetrization of meso-cyclohexendiol using BINAPO-Pd complex, Yoshizaki, H.; Satoh, H.; Sate, Y.; Nukui, S.; Shibasaki, M.; Mori, M. J. Org. Chem. 1995, 60, 2016.
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    • Significant dialkylation (32%) was occurred using (S)-BINAPO (38% yield, 57% ee of 13). See (a) Trost, B. M.; Murphy, D. J. Organometallics 1985, 4, 1143. (b) Mori, M.; Nukui, S.; Shibasaki, M. Chem. Lett. 1991, 1791. (c) For desymmetrization of meso-cyclohexendiol using BINAPO-Pd complex, Yoshizaki, H.; Satoh, H.; Sate, Y.; Nukui, S.; Shibasaki, M.; Mori, M. J. Org. Chem. 1995, 60, 2016.
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    • note
    • 3, F(000) = 2152, 4998 Independent reflections with I/σ(I) 2.0 were used on the analysis. Data for crystallographic analysis were measured on an Enraf-Nonius CAD-4 diffractormeter using graphite-monochromate MoKα (λ = 0.710 73 Å) and ω-2 scans in the range of θ; 1.36 < θ < 25.35. Structure was solved by direct methods and refined by least squares using the SHEL-X.


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