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Stereospecific alkylations of molybdenum(II) enolates from eta/sup 2/-aceyl complexes

Journal Article · · J. Am. Chem. Soc.; (United States)
DOI:https://doi.org/10.1021/ja00275a067· OSTI ID:5532964

The authors report here spectroscopic characterization and alkylation and aldol reactions of these Mo(II) enolate complexes as well as the structure of one diastereomer of (Tp')Mo(CO)(P(OPh)/sub 3/)(C(O)CHMEBz), Tp' = hydridotris(3,5-dimethylpyrazolyl)borate). Aldol condensation reactions of transition-metal enolates have not been reported as frequently as alkylation reactions. The authors find that metal enolate reacts with benzaldehyde to yield a deep indigo eta/sup 2/-enone derivative resulting from dehydration of the initial ..beta..-hydroxy eta/sup 2/-acyl product. The formation of (Tp')CO)/sub 2/Mo(eta/sup 2/-C(O)CMe = CHPh) (9) suggests that a range of electrophiles will react with these molybdenum(II) enolate reagents.

Research Organization:
Univ. of North Carolina, Chapel Hill
OSTI ID:
5532964
Journal Information:
J. Am. Chem. Soc.; (United States), Journal Name: J. Am. Chem. Soc.; (United States) Vol. 108:15; ISSN JACSA
Country of Publication:
United States
Language:
English