联菲双恶唑啉还可以用于催化其他的反应。
而且和苯环衍生的硫恶唑啉相比反应活性相对较高。
In addition, these ligands showed higher activity than thioether deveritives of phenyl oxazolines.
手性双恶唑啉是在不对称催化中广泛应用的一类重要的配体。
Chiral bisoxazolines have been widely applied ligands to asymmetric catalysis and a series of optically active bisoxazolines with rigid backbones and different chelate sizes were synthesized.
结果表明,用本文所述自由基悬浮聚合或本体聚合方法都能合成含恶唑啉环的活性聚苯乙烯。
The results showed reactive PS containing oxazoline ring could be synthesized by the suspension polymerization and bulk polymerization mentioned in this paper.
本文综述了手性双恶唑啉的合成及其金属配合物作为手性催化剂在催化不对称反应中的应用研究进展。
The synthesis and applications in catalytic asymmetric synthesis of C2-symmetric chiral bis (oxazoline) and its metal complexes are reviewed in this article.
以L—丝氨酸为原料,合成了旋光纯度很高的4(S)—2—甲基—4—甲氧羰基—2—恶唑啉单体。
A new optically active monomer of 4(S)—2—Methyl—4—Methoxycarbony1—2—Oxazoline has been synthesized from L—serine.
概括了近年来C_2轴手性双恶唑啉试剂及其金属络合物的合成及在催化不对称合成应用上的研究进展。
This review describes recent advances in the synthesis of C_2-symmetric chiral bis (oxazoline) ligands and the utility of its metal complexes in the catalysis of asymmetric syn - thesis.
用FTIR、DSC等方法研究了含恶唑啉官能团的聚苯乙烯(R PS)与氯化聚乙烯(CPE)之间的反应。
The reaction between polystyrene having oxazoline groups (RPS) and chlorinated polyethylene (CPE) was investigated by FTIR, DSC methods.
研究了(口恶)唑啉官能化聚苯乙烯(RPS)对聚酰胺66/聚对苯二甲酸乙二酯(PA 66/PET)共混物力学性能和相容性的影响。
The effects of PS with oxazoline functional group (RPS) on the mechanical properties and compatibility of PA 66/PET blends were studied.
本文简要介绍了新型唑啉类杀菌剂——恶咪唑及其富马酸盐,内容包括生物活性、应用、合成、专利等。
New fungicide named oxopoconazole was briefly reviewed in this paper. Its biological activities and performance, synthesis, patent status were also involved.
一个是亚磷酸三苯酯臭氧化合物,另一个是3-(4-硝基苯磺酰基)-2-苯基-2-硫代-1,3,2-恶唑磷啉。
One is triphenyl phosphite ozonide, the other is 3-(4-nitrophenylsulfonyl)-2-phenyl-2-thioxo-1,3,2-oxazaphospholidine.
一个是亚磷酸三苯酯臭氧化合物,另一个是3-(4-硝基苯磺酰基)-2-苯基-2-硫代-1,3,2-恶唑磷啉。
One is triphenyl phosphite ozonide, the other is 3-(4-nitrophenylsulfonyl)-2-phenyl-2-thioxo-1,3,2-oxazaphospholidine.
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