Allylsilanes in organic synthesis; stereoselective synthesis of trans-alkene peptide isosteres

Tetrahedron Letters

Volumn 36, Issue 41, 1995, Pages 7545-7548

  Daly, Matthew J ^a   Ward, Richard A ^a   Thompson, David F ^a   Procter, Garry ^a  

^a UNIVERSITY OF SALFORD   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ALKENE DERIVATIVE; PSEUDOPEPTIDE;

ARTICLE; DRUG SYNTHESIS; ENANTIOMER; REACTION ANALYSIS; STEREOCHEMISTRY;

EID: 0029157638     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/0040-4039(95)01528-0     Document Type: Article

References (23)

1. SN2? Ring opening of aziridines bearing an ?,?-unsaturated ester group with organocopper reagents. A new stereoselective synthetic route to (E)-alkene dipeptide isosteres
2. The stereochemistry of the reaction of allylsilanes with osmium tetroxide and of the epoxidation and methylenation of allylsilanes
3. The diastereoselectivity of electrophilic attack on trigonal carbon adjacent to a stereogenic centre: diastereoselective alkylation and protonation of open-chain enolates having a stereogenic centre carrying a silyl group at the ? position
4. The diastereoselectivity of electrophilic attack on trigonal carbon adjacent to a stereogenic centre: diastereoselective aldol reactions of open-chain enolates having a stereogenic centre carrying a silyl group at the ? position
5. Photochemistry of 2,3-di(1'-naphthyl)oxiranes. Spectral and kinetic behavior of carbonyl ylides in condensed media
6. Photochemistry of 2,3-di(1'-naphthyl)oxiranes. Spectral and kinetic behavior of carbonyl ylides in condensed media
7. An efficient synthesis of hydroxyethylene dipeptide isosteres: the core unit of potent HIV-1 protease inhibitors