Results 241 to 250 of about 210,494 (295)
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STRUCTURED GROUPS AND LINK-HOMOTOPY
Journal of Knot Theory and Its Ramifications, 1993We study link-homotopy classes of links in the three sphere using reduced groups endowed with peripheral structures derived from meridian-longitude pairs. Two types of peripheral structures are considered — Milnor’s original version (called “pre-peripheral structures” in Levine’s terminology) and Levine’s refinement (called simply “peripheral ...
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Inorganic Chemistry, 2009
Dimetallic compounds [(P-P)M(S(2)C(6)H(2)S(2))M(P-P)] (M = Ni, Pd; P-P = chelating bis(phosphine), 3a-3f) are prepared from O=CS(2)C(6)H(2)S(2)C=O or (n)Bu(2)SnS(2)C(6)H(2)S(2)Sn(n)Bu(2), which are protected forms of 1,2,4,5-benzenetetrathiolate. Selective monodeprotections of O=CS(2)C(6)H(2)S(2)C=O or (n)Bu(2)SnS(2)C(6)H(2)S(2)Sn(n)Bu(2) lead to [(P-P)
Kuppuswamy, Arumugam +6 more
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Dimetallic compounds [(P-P)M(S(2)C(6)H(2)S(2))M(P-P)] (M = Ni, Pd; P-P = chelating bis(phosphine), 3a-3f) are prepared from O=CS(2)C(6)H(2)S(2)C=O or (n)Bu(2)SnS(2)C(6)H(2)S(2)Sn(n)Bu(2), which are protected forms of 1,2,4,5-benzenetetrathiolate. Selective monodeprotections of O=CS(2)C(6)H(2)S(2)C=O or (n)Bu(2)SnS(2)C(6)H(2)S(2)Sn(n)Bu(2) lead to [(P-P)
Kuppuswamy, Arumugam +6 more
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Carbohydrate Research, 1996
A series of trisaccharide glycosides, Fuc-(1 reversible 2)-beta-Gal-(1 reversible 3)-beta-X-OMe (X = GlcNAc, Glc, 2-deoxy-Glc) related to the blood group determinant Le(d) have been synthesised both as their alpha- and beta-Fuc anomers together with the component disaccharide starting compounds.
J O, Duus +4 more
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A series of trisaccharide glycosides, Fuc-(1 reversible 2)-beta-Gal-(1 reversible 3)-beta-X-OMe (X = GlcNAc, Glc, 2-deoxy-Glc) related to the blood group determinant Le(d) have been synthesised both as their alpha- and beta-Fuc anomers together with the component disaccharide starting compounds.
J O, Duus +4 more
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Inorganic Chemistry, 2009
New pyridyl meso-tetraarylporphyrins (TArP, Ar = -C(6)H(4)-) of the general formula, T(R(1)R(2)NSO(2)Ar)P (R(1) = N-py-n-CH(2) (n = 2 or 4) and R(2) = CH(3)), have been synthesized by the versatile approach of utilizing meso-tetra(4-chlorosulfonylphenyl)porphyrin.
Janet, Manono +3 more
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New pyridyl meso-tetraarylporphyrins (TArP, Ar = -C(6)H(4)-) of the general formula, T(R(1)R(2)NSO(2)Ar)P (R(1) = N-py-n-CH(2) (n = 2 or 4) and R(2) = CH(3)), have been synthesized by the versatile approach of utilizing meso-tetra(4-chlorosulfonylphenyl)porphyrin.
Janet, Manono +3 more
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Evaluation and Program Planning, 2007
The California Youth Connection obtained funding from two foundations to evaluate the performance of group homes serving foster youth in Alameda County, California, in order to inform state policy-making. The evaluation team initially included 14 foster youth that personally experienced group home living.
Rex S, Green, Peter T, Ellis
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The California Youth Connection obtained funding from two foundations to evaluate the performance of group homes serving foster youth in Alameda County, California, in order to inform state policy-making. The evaluation team initially included 14 foster youth that personally experienced group home living.
Rex S, Green, Peter T, Ellis
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Optical properties and electronic structure of terminal group-perturbed ethynyl-linked dendrimers
Synthetic Metals, 2011Abstract Three ethynyl-linked dendrimers with terminal carbazole, namely the electronic donor–acceptor compounds 1–3 , the symmetric compound 9-(3-(2-(1-(2-(3-(9Hcarbazol-9-yl)-9-p-tolyl-9H-carbazol-6-yl)ethynyl)pyren-6-yl)ethynyl)-9-p-tolyl-9H-carbazol-6-yl)-9H-carbazole ( 1 ), the unsymmetric compounds 6-pyren-1-ylethynyl-9- p -tolyl-9 H -[3,9 ...
Peng Zhang +3 more
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Bioorganic & Medicinal Chemistry, 2008
Histone deacetylase (HDAC) inhibition is a recent, clinically validated therapeutic strategy for cancer treatment. Small molecule HDAC inhibitors identified so far fall in to three distinct structural motifs: the zinc-binding group (ZBG), a hydrophobic linker, and a recognition cap group.
Po C, Chen +4 more
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Histone deacetylase (HDAC) inhibition is a recent, clinically validated therapeutic strategy for cancer treatment. Small molecule HDAC inhibitors identified so far fall in to three distinct structural motifs: the zinc-binding group (ZBG), a hydrophobic linker, and a recognition cap group.
Po C, Chen +4 more
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Bioorganic & Medicinal Chemistry, 2015
The gene transfection efficiency (TE) of cationic lipids is largely influenced by the lipid structure. Six novel 1, 4, 7, 10-tetraazacyclododecane (cyclen)-based cationic lipids L1-L6, which contain double oleyl as hydrophobic tails, were designed and synthesized. The difference between these lipids is their diverse backbone.
Yi-Mei, Zhang +4 more
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The gene transfection efficiency (TE) of cationic lipids is largely influenced by the lipid structure. Six novel 1, 4, 7, 10-tetraazacyclododecane (cyclen)-based cationic lipids L1-L6, which contain double oleyl as hydrophobic tails, were designed and synthesized. The difference between these lipids is their diverse backbone.
Yi-Mei, Zhang +4 more
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‘To Link or not to Link?’ The Problem of the Multinational Enterprise Group Business Structure
2009AbstractAlthough enterprise groups are usually comprised of a bundle of separate legal entities, the traditional company law concepts of separate personality and limited liability might not match the economic reality of how groups operate. The question is therefore whether in dealing with group issues entity separateness should be kept for all purposes
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Dalton Transactions, 2008
Group 4 metallacycles [eta5:sigma-Me2C(C5H4)(C2B10H10)]Ti[eta2-N(Me)CH2CH2N(Me)] (1a), [eta5:sigma-Me2C(C5H4)(C2B10H10)]Zr[eta2-N(Me)CH2CH2N(Me)](HNMe2) (1b) and [eta5:sigma-Me2C(C5H4)(C2B10H10)]M[eta2-N(Me)CH2CH2CH2N(Me)] (M = Ti (2a), Zr (2b), Hf (2c)) were synthesized by reaction of [eta5:sigma-Me2C(C5H4)(C2B10H10)]M(NMe2)(2) (M = Ti, Zr, Hf) with ...
Mei-Mei, Sit +2 more
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Group 4 metallacycles [eta5:sigma-Me2C(C5H4)(C2B10H10)]Ti[eta2-N(Me)CH2CH2N(Me)] (1a), [eta5:sigma-Me2C(C5H4)(C2B10H10)]Zr[eta2-N(Me)CH2CH2N(Me)](HNMe2) (1b) and [eta5:sigma-Me2C(C5H4)(C2B10H10)]M[eta2-N(Me)CH2CH2CH2N(Me)] (M = Ti (2a), Zr (2b), Hf (2c)) were synthesized by reaction of [eta5:sigma-Me2C(C5H4)(C2B10H10)]M(NMe2)(2) (M = Ti, Zr, Hf) with ...
Mei-Mei, Sit +2 more
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