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271.
The isomerization polymerizations of glycidyl propionate (1b), octanoate (1c), and stearate (1d) with methylaluminum bis(2,6‐di‐tert‐butyl‐4‐methylphenoxide) (3) were investigated. The polymerizations selectively gave poly(2‐alkyl‐1,3‐dioxolane‐4,2‐diyloxymethylene)s (2), although the polymer yield as well as the polymer molecular weight significantly decreased as the acyl chain of 1 was lengthened. These polymers readily hydrolyzed to glycerin and the corresponding fatty acids under mild conditions. The copolymerizations of glycidyl acetate (1a) with these monomers were also examined. In any combination, the composition of the obtained copolymer was essentially identical with the feed ratio, while both copolymer yield and molecular weight decreased as the feed of 1a was decreased. © 1999 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 37: 435–444, 1999 (See graphics.)  相似文献   
272.
A C 2 -symmetrical phenol was used as a chiral auxiliary in the asymmetric aldol reaction of chiral acetates with various aldehydes [Eq. (a)]. The reaction proceeds readily under mild conditions to provide aldol adducts with high enantioselectivity. LDA=lithium diisopropylamide.  相似文献   
273.
A hydrophobic 96‐well multiplate was incubated with aqueous poly(uridine 5′‐p‐styrenesulfonate) (PUSS). Analysis of the PUSS‐coated surface indicated that the surface incubated at higher polymer concentration (50 mg·mL–1) was hydrophilic while the surface incubated at lower polymer concentration (1 mg·mL–1) was hydrophobic. Adhesion of 3T3‐L1, which has GalTase on the cell membrane, on the hydrophobic PUSS‐coated surface was greater than on the non‐coated surface. 3T3‐L1 adhesion on the hydrophilic PUSS‐coated surface was even greater. On the other hand, the adhesion of HeLa cells, which did not show GalTase on the cell membrane, on the hydrophilic surface was quite weak. It may well be said that the 3T3‐L1 adhesion on the hydrophilic PUSS‐coated surface was GalTase‐mediated.  相似文献   
274.
275.
13C NMR spectra of two poly(vinyl acetate)s (PVAC) with different tacticities (r‐diad, 0.54 and 0.57) were measured, and their peak intensities were compared with the calculated ones. The methine carbon signals were assigned with pentads in the order of mmmm, mmmr + rmmr, rmrr + mmrr, rrrr, mmrm, rmrm, mrrr, mrrm from low field. The methylene carbon signals were assigned with tetrads (partly with hexads) as rmr, rrr(mrrrm, mrrrr, rrrrr), mmr + mrr, mrm and mmm from low field. Some assignments are different from those previously reported. The methyl carbon signals showed splittings which were partly assigned.  相似文献   
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