In planta functions of cytochrome P450 monooxygenase genes in the phytocassane biosynthetic gene cluster on rice chromosome 2Ye, Z.; Yamazaki, K.; Minoda, H.; Miyamoto, K.; Miyazaki, S.; Kawaide, H.; Yajima, A.; Nojiri, H.; Yamane, H.; Okada, K.Biosci. Biotechnol. Biochem. 82, (2018).doi:10.1080/09168451.2017.1398067.
Synthesis and stereochemistry of JBIR-81, a peptide enamide derived from aspergilliKatsuta, R.; Toyoda, M.; Yajima, A.; Ishigami, K.; Nukada, T.Tetrahedron Letters 59, 1010-1013 (2018).doi:10.1016/j.tetlet.2018.01.080
2017年
Synthesis and stereochemistry of decarestrictines H and JKatsuta, R.; Masada, N.; Shimodaira, Y.; Ueda, S.; Yajima, A.; Nukada, T.Tetrahedron 73, 1733-1739 (2017).doi:10.1016/j.tet.2017.02.023
2016年
Synthesis and absolute configuration of formosusin A, a specific inhibitor of mammalian DNA polymerase βYajima, A.; Iizuka, Y.; Katsuta, R.; Nukada, T.Tetrahedron Lett. 57, 2012-2015 (2016).doi:10.1016/j.tetlet.2016.03.094
The Phytophthora mating hormone α2 is an antagonist of the counter hormone α1Zhang, L.; Yajima, A.; Ojika, M.Biosci. Biotechnol. Biochem. 80, 1062-1065 (2016).doi:10.1080/09168451.2016.1146071
How to calculate the number of stereoisomers of inositol homologsYajima, A.Bull. Chem. Soc. Jpn. 87, 1260-1264 (2014).doi:10.1246/bcsj.20140204
Computational Chemistry on Chemical GlycosylationsSatoh, H.; Nukada, T.Trends Glycosci. Glyc. 147, 11-27 (2014).doi:10.4052/tigg.26.11
Total synthesis of epicoccamides A and D via olefin cross-methathesisYajima, A.; Kawajiri, A.; Mori, A.; Katsuta, R.; Nukada, T.Tetrahedron Lett. 55, 4350-4354 (2014).doi:10.1016/j.tetlet.2014.06.040
Recent progress in the chemistry and chemical biology of microbial signaling molecules: quorum-sensing pheromones and microbial hormonesYajima, A.Tetrahedron Lett. 55, 2773-2780 (2014).doi:10.1016/j.tetlet.2014.03.051
Concise syntheses and biological activities of ganomycin I and fornicin AYajima, A.; Urao, S.; Katsuta, R.; Nukada, T.Eur. J. Org. Chem. 2014, 731-738 (2014).doi:10.1002/ejoc.201301269
2013年
Ubiquitin-specific peptidase 5, a target molecule of vialinin A, is a key molecule of TNF-alpha production in RBL- 2H3 cellsYoshioka, Y.; Ye, Y. Q.; Okada, K.; Taniguchi, K.; Yoshida, A.; Sugaya, K.; Onose, J.; Koshino, H.; Takahashi, S.; Yajima, A.; Yajima, S.; Abe, N.PLoS ONE 8, e80931doi:10.1371/journal.pone.0080931
Syntheses of 5′-O-desmethylterphenyllin and related p-terphenyls and their inhibitory activity of TNF-α release from RBL-2H3 cellsYajima, A.; Urao, S.; Yoshioka, S.; Abe, N.; Katsuta, R.; Nukada, T.Tetrahedron Lett. 54, 4986-4989 (2013).doi:10.1016/j.tetlet.2013.07.062
Vialinin A is a ubiquitin-specific peptidase inhibitorOkada, K.; Ye, Y. Q.; Taniguchi, K.; Yoshida, A.; Akiyama, T.; Yoshioka, Y.; Onose, J.; Koshino, H.; Takahashi, S.; Yajima, A.; Abe, N.; Yajima, S.Bioorg. Med. Chem. Lett. 23, 4328-4331 (2013).doi:10.1016/j.bmcl.2013.05.093
Total synthesis of virgineone aglycone and stereochemical assignment of natural virgineoneYajima, A.; Ida, C.; Taniguchi, K.; Murata, S.; Katsuta, R.; Nukada, T.Tetrahedron Lett. 54, 2497-2501 (2013).doi:10.1016/j.tetlet.2013.03.006
Synthesis of the core framework of the proposed structure of sargafuranKatsuta, R.; Aoki, K.; Yajima, A.; Nukada, T.Tetrahedron Lett. 54, 347-350 (2013). doi:10.1016/j.tetlet.2012.11.052
2012年
Determination of strain-specific wall teichoic acid structures in Lactobacillus plantarum reveals diverse α-d-glucosyl substitutions and high structural uniformity of the repeating units Tomita, S.; Furihata, K.; Tanaka, N.; Satoh, E.; Nukada, T.; Okada, S.Microbiol. 158, 2712-2723 (2012).doi:10.1099/mic.0.060913-0
Inhibitory effects of vialinin A and its analog on tumor necrosis factor-α release and production from RBL-2H3 cellsOnose, J.; Yoshioka, Y.; Ye, Q.; Sugaya, K.; Yajima, A.; Taniguchi, K.; Okada, K.; Yajima, S.; Takahashi, S.; Koshino, H.; Abe, N.Cell. Immunol. 279, 140-144 (2012).doi:10.1016/j.cellimm.2012.10.008
Synthetic study of versipelostatin A: Synthesis of the spirotetronate unit starting from pulegoneKatsuta, R.; Arai, K.; Yajima, A.; Nukada, T.Synlett 23, 397-400 (2012).doi:10.1055/s-0031-1290204
Structure-activity relationship of alpha hormones, the mating factors of phytopathogen PhytophthoraMolli, S. D., Qi, J.; Yajima, A.; Shikai, K.; Imaoka, T.; Nukada, T.; Yabuta, G.; Ojika, M.Bioorg. Med. Chem. 20, 681-686 (2012).doi:10.1016/j.bmc.2011.12.015
Synthesis of two osteoclast-forming suppressors, demethylincisterol A3 and chaxine AYajima, A.; Kagohara, Y.; Shikai, K.; Katsuta, R.; Nukada, T.Tetrahedron 68, 1729-1735 (2012).doi:10.1016/10.1016/j.tet.2011.12.057
2011年
Synthesis of the four stereoisomers of Phytophthora mating hormone alpha2 and a concise synthesis of mating hormone alpha1Yajima, A.; Toda, K.; Molli, S. D.; Ojika, M.; Nukada, T.Tetrahedron 2011, 67, 8887-8894.doi:10.1016/10.1016/j.tet.2011.09.066
Synthesis of aspergillide A via proline-catalyzed trans-to-cis isomerization of a substituted tetrahydropyranNagasawa, T.; Nukada, T.; Kuwahara, S.Tetrahedron 2011, 67, 2882-2888.doi:10.1016/j.tet.2011.02.061
Synthesis of microbial signaling molecules and thier stereochemistry-activity relationshipYajima, A.Biosci. Biotechnol. Biochem. 2011, 75, 1418-1429.doi:10.1271/bbb.110283
Synthesis of (±)-cyclic dehypoxanthine futalosine, the biosynthetic intermediate in an alternative biosynthetic pathway for menaquinonesYajima, A.; Kouno, S.; Dairi, T.; Mogi, M.; Katsuta, R.; Seto, H.; Nukada, T.Tetrahedron Lett. 2011, 52, 4934-4937.doi:10.1016/j.tetlet.2011.07.061
The second Phytophthora mating hormone defines interspecies biosynthetic crosstalkOjika, M.; Molli, S. D.; Kanazawa, H.; Yajima, A.; Toda, K.; Nukada, T.; Mao, H.; Murata, R.; Asano, T.; Qi, J.; Sakagami, Y.Nature Chemical Biology 2011, 7, 591-593.doi:10.1038/nchembio.617
Stereocontrolled total synthesis of (±)-3b-hydroxy-9b-pimara-7,15-diene, a putative biosynthetic intermediate of momilactonesYajima, A.; Toda, K.; Okada, K.; Yamane, H.; Yamamoto, M.; Hasegawa, M.; Katsuta, R.; Nukada, T.Tetrahedron Lett. 2011, 52, 3212-3215. doi:10.1016/j.tetlet.2011.04.044
