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Volumn 58, Issue 37, 2002, Pages 7381-7389

Enantioselective reduction of heteroaromatic β,γ-unsaturated ketones as an alternative to allylboration of aldehydes. Application: Asymmetric synthesis of SIB-1508Y

Author keywords

Allylboration; Enantioselective reduction; Ketone; SIB 1508Y

Indexed keywords

3 METHYL 5 (1 METHYL 2 PYRROLIDINYL)ISOXAZOLE; ALDEHYDE DERIVATIVE; KETONE DERIVATIVE; SIB 1508 Y; UNCLASSIFIED DRUG;

EID: 0037048456     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(02)00819-0     Document Type: Article
Times cited : (29)

References (47)
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    • DIP-chloride™ is the trademark of Aldrich Chemicals Company
    • (c) DIP-chloride™ is the trademark of Aldrich Chemicals Company.
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    • For a review of this field, see: (a) Carboni B., Vaultier M. Bull. Soc. Chim. Fr. 132:1995;1003-1008. and literature cited therein. For significant examples, see: (b) Salmon A., Carboni B. J. Organomet. Chem. 567:1998;6614-6617 (c) Waid P.P., Flynn G.A., Huber E.W., Sabol J.S. Tetrahedron Lett. 37:1996;4091-4094 (d) Evans D.A., Weber A.E. J. Am. Chem. Soc. 109:1987;7151-7157.
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    • For a review of this field, see: (a) Carboni B., Vaultier M. Bull. Soc. Chim. Fr. 132:1995;1003-1008. and literature cited therein. For significant examples, see: (b) Salmon A., Carboni B. J. Organomet. Chem. 567:1998;6614-6617 (c) Waid P.P., Flynn G.A., Huber E.W., Sabol J.S. Tetrahedron Lett. 37:1996;4091-4094 (d) Evans D.A., Weber A.E. J. Am. Chem. Soc. 109:1987;7151-7157.
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    • For a review of this field, see: (a) Carboni B., Vaultier M. Bull. Soc. Chim. Fr. 132:1995;1003-1008. and literature cited therein. For significant examples, see: (b) Salmon A., Carboni B. J. Organomet. Chem. 567:1998;6614-6617 (c) Waid P.P., Flynn G.A., Huber E.W., Sabol J.S. Tetrahedron Lett. 37:1996;4091-4094 (d) Evans D.A., Weber A.E. J. Am. Chem. Soc. 109:1987;7151-7157.
    • (1987) J. Am. Chem. Soc. , vol.109 , pp. 7151-7157
    • Evans, D.A.1    Weber, A.E.2


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