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Volumn 135, Issue 45, 2013, Pages 16853-16864

Enediolate-dilithium amide mixed aggregates in the enantioselective alkylation of arylacetic acids: Structural studies and a stereochemical model

Author keywords

[No Author keywords available]

Indexed keywords

ASYMMETRIC ALKYLATION; COMPUTATIONAL STUDIES; DENSITY FUNCTIONALS; ENANTIOSELECTIVE ALKYLATION; SOLUTION STRUCTURES; SPECTROSCOPIC STUDIES; STEREOCHEMICAL MODELS; STRUCTURAL STUDIES;

EID: 84884853720     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja403076u     Document Type: Article
Times cited : (51)

References (218)
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    • A comprehensive survey of scaled procedures used by Pfizer over two decades shows that 68% of all C-C bond formations are carbanion based and 44% of these involve enolates: Dugger, R. W.; Ragan, J. A.; Ripin, D. H. B. Org. Process Res. Dev. 2005, 9, 253
    • (2005) Org. Process Res. Dev. , vol.9 , pp. 253
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  • 8
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    • Green, J.R.1
  • 11
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    • Trost, B. M. Fleming, I. Pergamon: New York, Vol.
    • Caine, D. In Comprehensive Organic Synthesis; Trost, B. M.; Fleming, I., Eds.; Pergamon: New York, 1989; Vol. 1, p 1.
    • (1989) Comprehensive Organic Synthesis , vol.1 , pp. 1
    • Caine, D.1
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    • Dilithium amides showing structural analogies with 4 and their mixed aggregates have been studied computationally: Pratt, L. M.; Mu, R.; Carter, C.; Woodford, B. Tetrahedron 2007, 63, 1331
    • (2007) Tetrahedron , vol.63 , pp. 1331
    • Pratt, L.M.1    Mu, R.2    Carter, C.3    Woodford, B.4
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    • revision A.1; Gaussian, Inc. Wallingford, CT.
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