syn Stereocontrol in the directed dihydroxylation of acyclic allylic alcohols

Tetrahedron Letters

Volumn 40, Issue 38, 1999, Pages 6881-6885

  Donohoe, Timothy J ^a   Newcombe, Nicholas J ^b   Waring, Michael J ^a  

^a UNIVERSITY OF MANCHESTER   (United Kingdom)

^b ASTRAZENECA   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ACYCLIC HYDROCARBON SUBSTITUENT; ALCOHOL DERIVATIVE; ALKENE DERIVATIVE; ALLYL COMPOUND;

ARTICLE; CHEMICAL STRUCTURE; CHIRALITY; DIASTEREOISOMER; HYDROGEN BOND; HYDROXYLATION; MOLECULAR MODEL; OXIDATION; STEREOCHEMISTRY; STRUCTURE ACTIVITY RELATION;

EID: 0033578623     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(99)01371-4     Document Type: Article

References (15)

1. 4; a catalytic variant of the directed dihydroxylation process is under investigation.
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9. (b) Donohoe, T. J.; Moore, P. R.; Beddoes, R. L. J. Chem. Soc., Perkin Trans. 1 1997, 43.
10. 1H NMR spectroscopy and GC on the crude reaction mixture.
11. Donohoe, T. J.; Waring, M. J., unpublished work.
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13. For an interesting analogy see: Krysan, D. J.; Rockway, T. W.; Haight, A. R. Tetrahedron: Asymmetry 1994, 5, 625.
14. For a collection of the relevant data see: Adam, W.; Corma, A.; Reddy, I.; Renz, M. J. Org. Chem. 1997, 62, 3633.
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