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Analysis of revertants from respiratory deficient mutants within the centerNof cytochromebinSaccharomyces cerevisiae

Autor: Anne-Marie Colson, Hideto Miyoshi, Jean-Yves Coppée, J P di Rago, D Marc, N Tokutake

Publikováno v: FEBS Letters. 339:1-6

Four modified cytochrome b's carrying mononucleotide substitutions affecting center N residues were analysed. The mutant carrying a G33D change does not incorporate heme into the apocytochrome b and fails to grow on non-fermentable carbon sources. Ou

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::67be9c9a4d83b780188d6ca4c56a446d
https://doi.org/10.1016/0014-5793(94)80373-0

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Stereoselective reactions. XXXIV. Enantioselective deprotonation of prochiral 4-substituted cyclohexanones using chiral bidentate lithium amides having a bulky group instead of a phenyl group on the chiral carbon

Autor: M, Toriyama, K, Sugasawa, S, Motohashi, N, Tokutake, K, Koga

Publikováno v: Chemicalpharmaceutical bulletin. 49(4)

Using chiral bidentate lithium amides having a bulky group instead of a phenyl group on the chiral carbon, enantioselective deprotonation of prochiral 4-substituted cyclohexanones in the presence of excess trimethylsilyl chloride was examined in THF

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::d3bfd7ce57d7b561f4b892aa00dff891
https://pubmed.ncbi.nlm.nih.gov/11310676

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The absolute configuration of an intermediate cyclic sulfoximine in the asymmetric synthesis of transition-state analog inhibitors of γ-glutamylcysteine synthetase

Autor: N. Tokutake, A. Yamano, T. Irie, J. Hiratake, J.-I. Oda

Publikováno v: Acta Crystallographica Section C Crystal Structure Communications. 55:1598-1599

The crystal structure of a cyclic sulfoximine, 2-amino-4-(4-ethyl-1,3-dioxo-4,5-dihydro-1,2-thiazol-1-yl)butanoic acid, C 9 H 16 N 2 O 4 S, was determined to ascertain its stereochemistry. The absolute configuration of the chiral S atom was S on the

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::6374c4472be7c10ad563c51af0bb8b43
https://doi.org/10.1107/s0108270198016436

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