Authors: Yamagishi, T Suemune, K Yokomatsu, T Shibuya, S

Citation: T. Yamagishi et al., Diastereoselective synthesis of chiral beta-amino-alpha-hydroxy-H-phosphinates through hydrophosphinylation of alpha-amino aldehydes, TETRAHEDR L, 42(30), 2001, pp. 5033-5036

Authors: Yokomatsu, T Yamagishi, T Suemune, K Abe, H Kihara, T Soeda, S Shimeno, H Shibuya, S

Citation: T. Yokomatsu et al., Stereoselective reduction of cyclopropylalkaones possessing a difluoromethylenephosphonate group at the ring: Application to stereoselective synthesis of novel cyclopropane nucleotide analogues, TETRAHEDRON, 56(37), 2000, pp. 7099-7108

Authors: Yokomatsu, T Hayakawa, Y Suemune, K Kihara, T Soeda, S Shimeno, H Shibuya, S

Citation: T. Yokomatsu et al., Synthesis and biological evaluation of 1,1-difluoro-2-(tetrahydro-3-furanyl)ethylphosphonic acids possessing a N9-purinylmethyl functional group at the ring. A new class of inhibitors for purine nucleoside phosphorylases, BIOORG MED, 9(19), 1999, pp. 2833-2836

Authors: Yamagishi, T Yokomatsu, T Suemune, K Shibuya, S

Citation: T. Yamagishi et al., Enantioselective synthesis of alpha-hydroxyphosphinic acid derivatives through hydrophosphinylation of aldehydes catalyzed by Al-Li-BINOL complex, TETRAHEDRON, 55(41), 1999, pp. 12125-12136

Authors: Yokomatsu, T Abe, H Yamagishi, T Suemune, K Shibuya, S

Citation: T. Yokomatsu et al., Convenient synthesis of cyclopropylalkanol derivatives possessing a difluoromethylenephosphonate group at the ring, J ORG CHEM, 64(22), 1999, pp. 8413-8418

Authors: Yokomatsu, T Abe, H Sato, M Suemune, K Kihara, T Soeda, S Shimeno, H Shibuya, S

Citation: T. Yokomatsu et al., Synthesis of 1,1-difluoro-5-(1H-9-purinyl)-2-pentenylphosphonic acids and the related methano analogues. Remarkable effect of the nucleobases and thecyclopropane rings on inhibitory activity toward purine nucleoside phosphorylase, BIO MED CH, 6(12), 1998, pp. 2495-2505