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3 - tri s

Methyl-1-propanyl-3-ylidene) tris 2-(1,1-dimethylethyl)-5-methylphenol. See 1,1,3-Tri s (2-methyl -4-hydroxy-5-t-butyl phenyl) butane... [Pg.2680]

Polymer-supported BINOLs thus prepared were treated with Zr(Ot-Bu)4 to form polymer-supported zirconium 20. In the presence of 20 mol% of various zirconium 20, the model aza Diels-Alder reactions of imine Id with Danishefsky s diene (7a) were performed results from selected examples are shown in Table 5.8. Whereas the 4-t-butylphenyl group resulted in lower enantiomeric excess (ee), higher ee were obtained when 3,5-xylyl, 4-biphenyl, 4-fluorophenyl, and 3-tri-... [Pg.199]

The malonaldehyde thus formed can be estimated quantitatively by the thiobarbituric acid method (58, 59). As a control of the method s reliability, we used, as primary standard, 1, 3, 3-tri-ethoxypropene (46, 47) purified by gas-liquid chromatography (56) and hydrolyzed to malonaldehyde at room temperature with IN sulfuric acid. The molar... [Pg.114]

Nam 1-H, Y-M Kim, S Schmidt, Y-S Chang (2006) Biotransformation of 1,2,3-tri- and 1,2,3,4,7,8-hexachloro-dibenzo-p-dioxin by Sphingomonas wittichii strain RWl. Appl Environ Microbiol 72 112-116. [Pg.564]

C35H4206S4 4,5,6-Tri-0-benzoyl-2,3,-di-S-ethyl-2,3-dithio-D-allose diethyl TBETHA 38 482... [Pg.403]

X Example 4.3 Let s try another model with a slightly more complex input. Derive the state space representation of the differential equation... [Pg.66]

Fig. 3 Tris(0-substituted-xanthato)iron(III) (left X=0), tris(substituted-thioxanthato) iron(III) (left X=S), tris(substituted-dithioacetato)iron(III) (left X=CH2) and tris(disub-stituted-dithiophosphato)iron(III) (right)... Fig. 3 Tris(0-substituted-xanthato)iron(III) (left X=0), tris(substituted-thioxanthato) iron(III) (left X=S), tris(substituted-dithioacetato)iron(III) (left X=CH2) and tris(disub-stituted-dithiophosphato)iron(III) (right)...
Bi s(difluoroammo)-A -nitroethylamine, 0803 2-Cyano-l,2,3-tris(difluoroamino)propane, 1432 Di-l,2-bis(difluoroaminoethyl) ether, 1497 (Difluoroamino)difluoroacetonitrile, 0630... [Pg.125]

Figure 15 Examples of artificial collagen model peptide knots, (a) Regioselective artificial cystine knot, (b) dilysine scaffold,(c) c/s,c/s-1,3,5-trimethylcyclohexane-1,3,5-tricarboxylic acid Kemp tri acid , (d) TREN-(suc-OH)3, (Tris(2-aminoethyl)amine) succinic acid, (e) Fe + [2,2 -bipyridyl-peptide]3, " (f) monoalkyl chains, " (g) Boc-/3-Ala-TRIS-(OH)3 knot, and (h) N-terminal GFGEEG link. ... Figure 15 Examples of artificial collagen model peptide knots, (a) Regioselective artificial cystine knot, (b) dilysine scaffold,(c) c/s,c/s-1,3,5-trimethylcyclohexane-1,3,5-tricarboxylic acid Kemp tri acid , (d) TREN-(suc-OH)3, (Tris(2-aminoethyl)amine) succinic acid, (e) Fe + [2,2 -bipyridyl-peptide]3, " (f) monoalkyl chains, " (g) Boc-/3-Ala-TRIS-(OH)3 knot, and (h) N-terminal GFGEEG link. ...
Figure 3.1 Chemical structures of the current most successfully employed derivatised polysaccharide CSPs. (a) CHIRALPAK AD Amylose tris (3,5-dimethylphenylcarbamate) coated onto a silica support, (b) CHIRALPAK AS Amylose tris [(S)-a-methylbenzylcarbamate] coated onto a silica support, (c) CHIRALCEL OD Cellulose tris (3,5-dimethylphenylcarbamate) coated onto a silica support, (d) CHIRALCEL OJ Cellulose tris (4-methylbenzoate) coated onto a silica support. Figure 3.1 Chemical structures of the current most successfully employed derivatised polysaccharide CSPs. (a) CHIRALPAK AD Amylose tris (3,5-dimethylphenylcarbamate) coated onto a silica support, (b) CHIRALPAK AS Amylose tris [(S)-a-methylbenzylcarbamate] coated onto a silica support, (c) CHIRALCEL OD Cellulose tris (3,5-dimethylphenylcarbamate) coated onto a silica support, (d) CHIRALCEL OJ Cellulose tris (4-methylbenzoate) coated onto a silica support.
A similar strategy has been employed in the synthesis of a dihydropyran required to achieve the synthesis of (—)-lanlimalide (Scheme 23). Thns, ally-lation of the secondary alcohol resnlting from a methallylation of 3-tri-n-butylstannylacrolein provided unsymmetrical ether 182, which is closed to a pyran with a ring-closing metathesis using Schrock s molybdennm catalyst. [Pg.66]

Newton s method is only guaranteed to converge for initial estimates that are sufficiently close to a solution. To see this for yourself, try applying Newton s method to find values of x for which g(x) = tan 1 x = 0. In this case, Newton s method is xl+ = x, (1 + xf) tan 1 x,. Explore how well this method converges for initial estimates including xo = 0.1,xo = 1, and... [Pg.79]


See other pages where 3 - tri s is mentioned: [Pg.441]    [Pg.273]    [Pg.355]    [Pg.441]    [Pg.273]    [Pg.355]    [Pg.54]    [Pg.382]    [Pg.2364]    [Pg.88]    [Pg.10]    [Pg.483]    [Pg.1191]    [Pg.50]    [Pg.274]    [Pg.272]    [Pg.252]    [Pg.222]    [Pg.289]    [Pg.48]    [Pg.293]    [Pg.294]    [Pg.191]    [Pg.29]    [Pg.565]    [Pg.129]    [Pg.191]    [Pg.92]    [Pg.237]    [Pg.617]    [Pg.57]    [Pg.58]   
See also in sourсe #XX -- [ Pg.86 ]

See also in sourсe #XX -- [ Pg.86 ]




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Borohydrides, tri-s-butylreduction

Borohydrides, tri-s-butylreduction unsaturated carbonyl compounds

Hexahydro-1,3,5-tri s-triazine

Hexahydro-1,3,5-tris(2-hydroxyethyl)s-triazine

Lithium tri-s-butylborohydride

Potassium tri-s-butylborohydride

Tris -s-triazine, as reference compound for mass spectrometry

Tris- -s-triazine

Tris- -s-triazme

Wilkinson’s catalyst tris

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