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1 for (14R, 15S)-epoxyeicosatrienoic acid (76% optical purity).
2 opargylic fluorides, respectively, with high optical purity.
3 ective for the generation of BINOL with high optical purity.
4 of pharmaceutical importance with excellent optical purity.
5 o generate allenes in good yield and in high optical purity.
6 n nearly quantitative yield, without loss of optical purity.
7 ld be recovered in 95% yield with no loss in optical purity.
8 s to obtain the desired S-enantiomer in high optical purity.
9 3c) were asymmetrically synthesized in high optical purity.
10 d to the corresponding alcohols in excellent optical purity.
11 nantiomeric composition and was equated with optical purity.
12 tom led to the cyclization product with high optical purity.
13 ti-Prelog configurated alcohols in excellent optical purity.
14 m quaternary stereocenter, in high yield and optical purity.
15 acid target compound in >99.9% chemical and optical purity.
16 alyte is only available in one form of known optical purity.
17 to excellent chemical yield without loss of optical purity.
18 ich affords both enantiomers of each in high optical purity.
19 abolite (S)-cotinine were prepared with high optical purity.
20 d alcohols can be coupled without erosion of optical purity.
21 , which was converted to 7 with retention of optical purity.
22 1 were derived from l-pipecolic acid in 96% optical purity.
23 ion operations on intermediates to raise the optical purity.
24 ve cyclization can be accomplished with high optical purities.
25 o-beta-hydroxy ester diastereomers with high optical purities.
26 ven-membered heterocyclic products with high optical purities.
27 rnished in exceptional conversions (88%) and optical purity (99% ee) and serves as an intermediate fo
28 intermediates of CBI in good conversions and optical purity (99% ee), and provided an alternative app
29 ith vicinal quaternary stereocenters in high optical purity and as single diastereoisomers is now rep
30 l nonracemic biaryl compounds with excellent optical purity and good isolated chemical yields (in mos
34 anthanide shift reagent Eu(fod)(3) indicated optical purity, and the (4S,2'R)-configuration was assig
35 rmation of (8R,9S)-epoxyeicosatrienoic acid (optical purities are 91 and 90% for CYP2N1 and CYP2N2, r
36 ly) and (11R, 12S)-epoxyeicosatrienoic acid (optical purities are 92 and 70% for CYP2N1 and CYP2N2, r
38 were obtained on a multigram scale in > 99% optical purity by optical resolution of the racemate wit
40 alcohols, experience very little erosion of optical purity by way of redox equilibration under the c
41 tive stereochemistry as well as the changing optical purity can be effectively rationalized by transi
42 of the fragment ion abundance ratio and the optical purity, characteristic of the kinetic method, al
43 of a beta-keto tertiary amide, which retains optical purity enabled by A(1,3)-strain rendering slow e
44 arallel with conventional chemistry and high optical purity for complex compounds with multiple chira
45 (>20:1 in all cases examined), no erosion in optical purity for proximal stereogenic centers, and a t
46 carboxylate iodides were synthesized in high optical purities from (R)-(-) and (S)-(+)-1,4-dihydro-2,
47 s and proceeds in 83% overall yield and >99% optical purity from readily available starting materials
50 ablished synthetic procedures due to loss of optical purity in the key step, i.e., the Barton-Kellogg
52 amino acid was synthesized in high yield and optical purity in three steps from readily available sta
53 of the fragment ion abundance ratio and the optical purity (intrinsic to the kinetic method) allows
54 showed that crosslinked SCRII gave a product optical purity of 100% and a yield of >99.9% within 3 h,
56 e observed for alkyl-substituted imines, the optical purity of the aziridines from all of the imine s
58 to guarantee selectivity of the reaction and optical purity of the target compounds, simplifying the
59 traenoic acid (>/=99% of total products, 97% optical purity), P450BM-3 is only moderately regioselect
61 D-phenylalanines in high yield and excellent optical purity, starting from inexpensive cinnamic acids
62 herein afford various cyclic amines of high optical purity; such products are not easily accessed by
63 o-aminoalkenes provides products with higher optical purities than obtained with N-proteo-aminoalkene
64 es only one sample of the analyte with known optical purity to allow construction of a calibration cu
65 uaternary arylglycines were prepared in high optical purity (up to 98% ee) by alpha-alkylation of dep
66 arylethanols were synthesized with excellent optical purity via enzymatic reduction of the correspond
67 2'R) enantiomers of 1 were obtained in > 99% optical purity while the (2S,2'S) and (2R,2'S) enantiome
68 -sparteine and O'Brien's diamine give higher optical purities with VANOL and VAPOL than with BINOL, a
69 een synthesized in five steps with excellent optical purity with approximately 99% ee and >99% de.
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