Dispiroketals in synthesis (part 10): Further reactions of dispoke protected lactate and glycolate enolates

Tetrahedron

Volumn 50, Issue 24, 1994, Pages 7157-7176

  Boons, Geert Jan ^a   Downham, Robert ^a   Kim, Kun Soo ^a   Ley, Steven V ^a   Woods, Martin ^a  

^a UNIVERSITY OF CAMBRIDGE   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ESTER DERIVATIVE; HYDROXYACID; SPIRO COMPOUND;

ARTICLE; DRUG SYNTHESIS; ENANTIOMER; PRIORITY JOURNAL; REACTION ANALYSIS;

EID: 0028284175     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(01)85241-8     Document Type: Article

References (16)

1. 616. The resolution and reactions of tertiary alcohols: two disubstituted glycollic acids and the corresponding disubstituted glycols
2. Dispiroketals in synthesis (part 6): Highly stereoselective alkylation of dispiroketal protected lactate and glycolate enolates
3. Substitution of HMPT by the cyclic urea DMPU as a cosolvent for highly reactive nucleophiles and bases
4. Stereochemical Studies. XVII. Nitrous Acid Deaminations of (R)-α-Methylphenylalanine and Its Methyl Ester in Acetic Acid
5. New epoxidation with m-chloroperbenzoic acid at elevated temperatures