ChemInform Abstract: NEW AND IMPROVED SYNTHESIS OF OPTICALLY PURE (R)- AND (S)-2,2′-DIMETHYL-1,1′-BINAPHTHYL AND RELATED COMPOUNDS

1985 ◽  
Vol 16 (34) ◽  
Author(s):  
N. MAIGROT ◽  
J.-P. MAZALEYRAT
ChemInform ◽  
2010 ◽  
Vol 31 (27) ◽  
pp. no-no
Author(s):  
Masashi Sugiya ◽  
Hiroyuki Nohira

Synthesis ◽  
1985 ◽  
Vol 1985 (03) ◽  
pp. 317-320 ◽  
Author(s):  
Nicole Maigrot ◽  
Jean-Paul Mazaleyrat

2003 ◽  
Vol 68 (5) ◽  
pp. 931-950 ◽  
Author(s):  
Marcela Krečmerová ◽  
Miloš Buděšínský ◽  
Milena Masojídková ◽  
Antonín Holý

Reaction of ethyl (R)-oxiranecarboxylate (2a) with various nucleobases (adenine, 6-chloropurine, thymine, cytosine, N6-benzoyladenine, 4-methoxy-5-methylpyrimidin-2(1H)-one and 4-methoxypyrimidin-2(1H)-one) afforded ethyl 3-substituted-2-hydroxypropanoates 4-10. Enantioselectivity of this reaction is dependent on the type of the base: 6-chloropurine, N6-benzoyladenine, 4-methoxy-5-methylpyrimidin-2(1H)-one, thymine and cytosine gave optically pure R enantiomers. In other cases, partial or complete racemization occurred. Optically pure ethyl (R)-3-(6-chloropurin-9-yl)-2-hydroxypropanoate (5a) was hydrolyzed to give (R)-3-(6-chloropurin-9-yl)-2-hydroxypropanoic acid (11). Reactions of 11 with various primary or secondary amines led to N6-substituted (R)-3-(adenin-9-yl)-2-hydroxypropanoic acids 14-19. Enantiomeric purity was determined from 1H NMR spectra measured in the presence of (-)-(R)-1-(9-anthryl)-2,2,2-trifluoroethan-1-ol.


1989 ◽  
Vol 67 (12) ◽  
pp. 2089-2094 ◽  
Author(s):  
William A. Ayer ◽  
Masayuki Kamada ◽  
Yu-Ting Ma

The metabolites of several strains of a fungus that gives rise to the disease of conifers known as Sirococcus shoot blight have been studied. The metabolites are similar to those isolated from Gremmeniellaabietina, the causative agent of Scleroderris canker of pine. Sclerodin (1), scleroderolide (2), and Scleroderris blue (3) have been isolated, along with the known lactone 4, trypethelone (6), and a new purple compound named scleroquinone (12). Another new compound, related to Scleroderris blue (3) and Scleroderris green (7); which we have named Scleroderris yellow, is shown to possess structure 8. The sclerodin (1) isolated in these studies is not optically pure, in some cases being nearly racemic. It is noted that the optical purity may be a function of the culture medium employed. Scleroderolide (2) strongly inhibits the germination of lettuce seeds. In addition to the metabolites noted, squalene, methyl oleate, stearic acid, ergosta-4,6,8(14),22-tetraene-3-one, and ergosterol endoperoxide were also isolated from the cultures. Keywords: Sirococcus, phenalenones, Scleroderris yellow, scleroquinone, sclerodin.


2001 ◽  
Vol 79 (5-6) ◽  
pp. 731-741 ◽  
Author(s):  
Paul Beagley ◽  
Philip Davies ◽  
Harry Adams ◽  
Colin White

The syntheses of the chiral ansa-metallocene complexes TiCl2(η5:η5-C5Me4SiMe2C5H3R*) (R* = menthyl (4a) or neomenthyl (4b)) are reported; initially 4a was obtained as a 3:1 mixture of (R:S) diastereoisomers, which differ only in which face of the asymmetrically substituted cyclopentadienyl ring is bonded to the titanium (chiral descriptor shown). The major diastereomer 4aR was crystallized out optically pure from the initial reaction mixture, whereas the 4aS diastereoisomer was isolated after isomerizing a racemic mixture of 4a to a 1:3 mixture of (R:S) diastereoisomers using UV irradiation. The corresponding neomenthyl complex 4b was obtained as a 1.3:1 mixture of diastereoisomers that could not be separated. The optically pure 4aR was converted stereoselectively into the corresponding (R)-TiMe2(η5:η5-C5Me4SiMe2C5H3R*) (R* = menthyl). Syntheses of the related indenyl ligand system C5Me4SiMe2C9H7 (3) is reported but complexation to titanium proved to be problematic although ZrCl2(η5:η5-C5Me4SiMe2C9H6) (6) was isolated. The crystal structures of both 4aR and 4aS are reported and compared. Crystals of 4aR are orthorhombic, a = 27.857(11), b = 9.985(5), and c = 9.596(4) Å, Z = 4, space group P212121 (D24, No. 19), and those of 4aS are monoclinic, a = 8.5810(10), b = 38.679(4), and c = 8.5842(10) Å, β = 113.001(2)°, Z = 4, space group P21 (C22, No. 4). The structures were solved by the Patterson method and 4aR was refined by blocked-cascade least-squares procedures to R = 0.0628 (Rω = 0.0503) for 902 reflections with |F|/σ(|F|) [Formula: see text] 3.0, whereas 4aS was refined by full-matrix least-squares procedures to R = 0.0646 (wR2 = 0.1829) for 5734 reflections with |F|/σ(|F|) [Formula: see text] 4.0. Both diastereomers of 4a catalyze hydrosilylation of ketones, but as expected from a comparison of the two crystal structures, the 4aR isomer is the more stereoselective catalyst, i.e., hydrosilylation of acetophenone followed by hydrolysis gives 82% enantiomeric excess (ee) of (S)-PhCH(Me)OH with 4aR whereas only 16% ee of (R)-PhCH(Me)OH with 4aS.Key words: titanium, metallocene, chiral, structure, catalyst.


Sign in / Sign up

Export Citation Format

Share Document