排序方式: 共有20条查询结果,搜索用时 31 毫秒
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Hodgson DM Kirton EH Miles SM Norsikian SL Reynolds NJ Coote SJ 《Organic & biomolecular chemistry》2005,3(10):1893-1904
Organolithium-induced deprotonation of terminal epoxides in the presence of appropriate diamine ligands allows trapping with a range of electrophiles, yielding functionalised di- and tri-substituted epoxides in good yields and with control of stereochemistry at the epoxide. 相似文献
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The asymmetric Michael addition of glycine imine esters to simple α,β-unsaturated ketones via PTC is investigated. It is found that by employing 1 mol % of a chiral quaternary ammonium salt, derived from α-methylnaphthylamine in conjunction with Cs2CO3, high enantioselectivities can be obtained in conjugate additions involving simple alkylvinylketones. 相似文献
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Hodgson DM Buxton TJ Cameron ID Gras E Kirton EH 《Organic & biomolecular chemistry》2003,1(23):4293-4301
Enantioselective alpha-deprotonation of achiral epoxides 1, 21, and 26 using organolithiums in the presence of (-)-sparteine 2 and subsequent electrophile trapping gives access to enantioenriched trisubstituted epoxides 9-17, 22, 23, 27 and 28 (in up to 86% ee). 相似文献
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We show that the wide distribution of time constants required to explain 1/ƒ noise in MOSFETs arises as a natural consequence of the multi-phonon model of carrier trapping into individual Si-SiO2 interface states. A new class of random telegraph signal found in the drain current of small-area silicon MOSFETs is described. These signals are a result of defect metastability and are shown to be a source of non-Gaussian noise. 相似文献
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Angie?S?Mah Andrew?EH?Elia Geeta?Devgan Jason?Ptacek Mike?Schutkowski Michael?Snyder Michael?B?Yaffe Raymond?J?DeshaiesEmail author 《BMC biochemistry》2005,6(1):22
Background
The mitotic exit network (MEN) is a group of proteins that form a signaling cascade that is essential for cells to exit mitosis in Saccharomyces cerevisiae. The MEN has also been implicated in playing a role in cytokinesis. Two components of this signaling pathway are the protein kinase Dbf2 and its binding partner essential for its kinase activity, Mob1. The components of MEN that act upstream of Dbf2-Mob1 have been characterized, but physiological substrates for Dbf2-Mob1 have yet to be identified. 相似文献8.
In this paper we present results of a study into whether the tricyclic core of the lepadiformines A-C can be accessed via intramolecular hetero-Diels-Alder cycloaddition. We are able to demonstrate that such a process is possible and that the reaction proceeds in an endo-selective fashion, providing the correct relative stereochemistry for this family of natural products. By employing this approach we have been able to develop a short (7 step) synthesis of (+/-)-lepadiformine A, starting from commercially-available trans-2-nonenal. 相似文献
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