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J Uenishi

Showing results (1-10 of 6) with videos related to

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Nucleic Acids Symposium Series|January 1, 1992
Preparation of thianucleoside derivativesJ Uenishi, M Motoyama, K Takahashi
Nucleic Acids Symposium Series|January 1, 1993
Synthesis of 4'-methyl-4'-thiothymidineJ Uenishi, H Kawanami, Y Kubo
Chemical & Pharmaceutical Bulletin|December 1, 1975
Chemical structure and sweet taste of isocoumarin and related compounds. VIM Yamato, K Hashigaki, J Uenishi, et al.
Chemical & Pharmaceutical Bulletin|May 13, 1999
Total synthesis of (+/-)-acetomycin and design of esterase-resistant analogsJ Uenishi, N Kobayashi, S Komine, et al.
Chemical & Pharmaceutical Bulletin|April 23, 1999
Synthetic studies of the 18-membered antitumor macrolide, tedanolide. 3. Stereocontrolled synthesis of the C1-C12 part via a synthesis of the C1-C7 fragment by a mismatched but efficient sharpless dihydroxylation and its coupling with the C8-C11 fragmentT Matsushima, M Mori, B Z Zheng, et al.
Chemical & Pharmaceutical Bulletin|October 12, 1999
Synthetic studies of an 18-membered antitumor macrolide, tedanolide. 5. Stereoselective synthesis of the C13-C23 part via condensation of two fragments, C13-C17 and C18-C21, by taking advantage of the 3,4-dimethoxybenzyl protecting groupB Z Zheng, H Maeda, M Mori, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Nucleic Acids Symposium Series|January 1, 1992
Preparation of thianucleoside derivativesJ Uenishi, M Motoyama, K Takahashi
Nucleic Acids Symposium Series|January 1, 1993
Synthesis of 4'-methyl-4'-thiothymidineJ Uenishi, H Kawanami, Y Kubo
Chemical & Pharmaceutical Bulletin|December 1, 1975
Chemical structure and sweet taste of isocoumarin and related compounds. VIM Yamato, K Hashigaki, J Uenishi, et al.
Chemical & Pharmaceutical Bulletin|May 13, 1999
Total synthesis of (+/-)-acetomycin and design of esterase-resistant analogsJ Uenishi, N Kobayashi, S Komine, et al.
Chemical & Pharmaceutical Bulletin|April 23, 1999
Synthetic studies of the 18-membered antitumor macrolide, tedanolide. 3. Stereocontrolled synthesis of the C1-C12 part via a synthesis of the C1-C7 fragment by a mismatched but efficient sharpless dihydroxylation and its coupling with the C8-C11 fragmentT Matsushima, M Mori, B Z Zheng, et al.
Chemical & Pharmaceutical Bulletin|October 12, 1999
Synthetic studies of an 18-membered antitumor macrolide, tedanolide. 5. Stereoselective synthesis of the C13-C23 part via condensation of two fragments, C13-C17 and C18-C21, by taking advantage of the 3,4-dimethoxybenzyl protecting groupB Z Zheng, H Maeda, M Mori, et al.
Pageof 1