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91.
The synthesis and characterization by 1H, 13C, 119Sn NMR and 119Sn Mössbauer spectroscopy of (Z)-1-[2-(triphenylstannyl)vinyl]-1-cycloheptanol,

(1), and (Z)-1-[2-tri-p-tolylstannyl)vinyl-1-cycloheptanol,

(2), are described, together with their halodemetallation by I2, Br2 and ICIl to yield derivatives of the types

(Ar = phenyl or p-tolyl, N = 1, 2; X = I, Br, Cl, respectively). The solid-state structures of four compounds have been determined by X-ray diffraction analysis. In the crystals of

(1) and

(2) the Sn atom has a tetrahedral geometry distorted towards trigonal bipyramid as a consequence of a close intramolecular contact with the hydroxyl O(1) atom of 2.742(3) Å and 2.768(3) Å, respectively. A trigonal bipyramidal geometry is found in

(12) and

(4), in which significant Sn---O(1) interactions are noted [2.437(8) Å and 2.407(8) Å, respectively].  相似文献   
92.
We define a quantum-algebra associated to as an associative algebra depending on two parameters. For special values of the parameters, this algebra becomes the ordinary-algebra of , or theq-deformed classical-algebra algebra of . We construct free field realizations of the quantum-algebra and the screening currents. We also point out some interesting elliptic structures arising in these algebras. In particular, we show that the screening currents satisfy elliptic analogues of the Drinfeld relations in.The research of the second author was partially supported by NSF grant DMS-9501414.  相似文献   
93.
94.
In 1962 Erd\H{o}s proved that every real number may be decomposed into a sum of Liouville numbers. Here we consider more general functions which decompose elements from an arbitrary local field into Liouville numbers. Several examples and applications are given. As an illustration, we prove that for any real numbers , not equal to 0 or 1, there exist uncountably many Liouville numbers such that are all Liouville numbers.

  相似文献   

95.
96.
The development of a one-pot tandem intramolecular conjugate addition/nucleophilic acyl substitution using samarium(II) iodide is reported. The reaction relies on the reagent’s unique ability to mediate both radical and anionic pathways, which are likely integral to the mechanism of this transformation. The tricyclic hemiacetal product was formed in good yield, with excellent diastereoselectivity, and its structure was verified by X-ray crystallographic analysis.  相似文献   
97.
98.
In an unprecedented transformation, amide ligands are found to attack the imine carbon centers of tridentate Schiff base ligands attached to tin. The process is reversible, and the resultant (masked) amide species can be exploited as latent single-site initiators for the controlled polymerization of rac-lactide.  相似文献   
99.
Asymmetric [2,3]-rearrangement of glycine-derived allyl ammonium ylids   总被引:1,自引:0,他引:1  
The first examples of highly enantioselective [2,3]-sigmatropic rearrangements of acyclic allylic ammonium ylids are reported. Thus, a range of N-{2'-[(N'-allyl-N',N'-dialkyl)ammonium]}acetyl camphor sultams undergo rearrangement at 0 degrees C in DME solution with high diastereofacial control (up to 99:1 dr) to give allylglycines in generally high yield. The power of the method has been demonstrated in a rapid and efficient synthesis of (R)-allyl glycine.  相似文献   
100.
1 INTRODUCTION Many plants contain proteins that are capable of inactivating ribosomes and therefore are called ribosome-inactivating proteins or RIPs[1]. RIPs are RNA N-glycosidases that inactivate ribosomes through a site-specific deadenylation of the large ribosomal RNA[2, 3]. RIPs are also capable of inactivating many nonribosomal nucleic acid substrates and can be considered as polynucleotide: adenosine glycosidases[4~6]. There are two types of RIPs: type I, single chain pr…  相似文献   
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