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Glycine-derived silyl enolates

The Zr-BINOL catalyst system provides an efficient synthetic method of anti-p-hydroxy-a-amino acid derivatives (23) using glycine-derived silyl enolates (22)... [Pg.299]

Use of the preformed Z-silyl enol ether 18 results in quite substantial anti/syn selectivity (19 20 up to 20 1), with enantiomeric purity of the anti adducts reaching 99%. The chiral PT-catalyst 12 (Schemes 4.6 and 4.7) proved just as efficient in the conjugate addition of the N-benzhydrylidene glycine tert-butyl ester (22, Scheme 4.8) to acrylonitrile, affording the Michael adduct 23 in 85% yield and 91% ee [10]. This primary product was converted in three steps to L-ornithine [10]. The O-allylated cinchonidine derivative 21 was used in the conjugate addition of 22 to methyl acrylate, ethyl vinyl ketone, and cydohexenone (Scheme 4.8) [12]. The Michael-adducts 24-26 were obtained with high enantiomeric excess and, for cydohexenone as acceptor, with a remarkable (25 1) ratio of diastereomers (26, Scheme 4.8). In the last examples solid (base)-liquid (reactants) phase-transfer was applied. [Pg.50]

As shown in Scheme 8.2, chiral P-hydroxy-a-amino adds can be obtained by the Mukaiyama-type aldol reaction of aldehydes with glycine-derived enol silyl ethers using cinchona-based quaternary ammonium salts. In 2004, Castle and coworkers [9] found that dnchona-based quaternary ammonium salts such as 13 are also able to catalyze the dired aldol readion of aldehydes with the glydne donor 14 in the presence of a phosphazene base such as BTTP (t-butyliminotri(pyrrolidino)phos-... [Pg.200]

The nucleophilic attack of silyl enol glycine derivative to a dienyl acetate organometallic complex proceeds readily and regio-specifically at —78 °C in the presence of TMSOTf to afford a dienyl glycine derivative in excellent yield (eq 1IQ). ... [Pg.539]

Williams and Rastetter also accomplished an elegant synthesis of ( )-hyalodendrin (83) in 1980 [39]. Beginning with the sarcosine anhydride-derived enolic aldehyde 78, silyl protection of the enal enabled alkylation of the glycine center with benzyl bromide and thiolation using LDA and monoclinic sulfur a la Schmidt. After protection of the thiol with methylsulfenyl chloride and deprotection of the silyl ether, the enol was sulfenylated with triphenylmethyl chlorodisulfide to afford bis(disulfide) 82 as a 2 1 mixture of diastereomers favoring the anti isomer. Reduction of the disulfides with sodium borohydride and oxidation with KI3 in pyridine afforded ( )-hyalodendrin (83) in 29 % yield (Scheme 9.4). [Pg.222]

Transmetalation of the ( )-0-Li-enolate derived from the stabase -protected glycine ethyl ester (11) with 1.1 equiv of (1) affords the chiral Ti enolate (12), which adds with high re selectivity to various aldehydes. By mild acidic cleavage of the silyl protecting group, the primary product (13) can be transformed to various Af-derivatives (14) of D-t/treo-a-amino-p-hydroxy acids in 45-66% yield and with excellent enantio- and syn(threo) selectivity (97-99%) (eq 3). An exception with lower enantioselectivity is glyoxylic ester (ethyl ester 78% ee t-butyl ester 87% ee). [Pg.190]

Masamune et al. examined the catalytic activity of several boron Lewis acids derived from BH3 THF and the p-toluenesulfonamides of simple a-amino acids towards the aldol reaction of benzaldehyde with TMS enolate 48 [121]. As a result, the borane catalysts derived from a,a-disubstituted glycine p-tolueriesulforiarriides were found to have high activity. The disubstitution would accelerate the second step (Step II) of the catalytic cycle (Scheme 10.43). On the basis of this observation, they developed chiral borane catalysts 47 c and 47 d, which enable highly enantioselective aldol reactions of KSA and thioketene silyl acetals (84—99% ee with 48). [Pg.437]


See other pages where Glycine-derived silyl enolates is mentioned: [Pg.528]    [Pg.146]    [Pg.249]    [Pg.1821]    [Pg.193]    [Pg.669]    [Pg.317]   


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Enolates silylation

Glycine derivatives

Glycine-derived enol silyl ethers

Silyl derivatives

Silyl enolate

Silyl enolates

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