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C Kabuto

Showing results (1-10 of 5) with videos related to

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Nature|March 1, 2003
A stable silicon-based allene analogue with a formally sp-hybridized silicon atomS Ishida, T Iwamoto, C Kabuto, et al.
Science (New York, N.Y.)|October 20, 2000
A stable bicyclic compound with two Si=Si double bondsT Iwamoto, M Tamura, C Kabuto, et al.
Planta Medica|July 1, 1981
Structure of methyl adenophorate and triphyllol, triterpenoids of Adenophora triphylla var. japonica rootsC Konno, T Saito, Y Oshima, et al.
The Journal of Organic Chemistry|October 13, 2001
Formation of cyclic ethers via the palladium-catalyzed cycloaddition of activated olefins with allylic carbonates having a hydroxy group at the terminus of the carbon chainM Sekido, K Aoyagi, H Nakamura, et al.
Chemical & Pharmaceutical Bulletin|July 18, 2001
Diels-Alder cycloadditions of 2(1H)-quinolones having an electron-withdrawing group at the 3-position acting as dienophiles with dienesR Fujita, K Watanabe, T Yoshisuji, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
Nature|March 1, 2003
A stable silicon-based allene analogue with a formally sp-hybridized silicon atomS Ishida, T Iwamoto, C Kabuto, et al.
Science (New York, N.Y.)|October 20, 2000
A stable bicyclic compound with two Si=Si double bondsT Iwamoto, M Tamura, C Kabuto, et al.
Planta Medica|July 1, 1981
Structure of methyl adenophorate and triphyllol, triterpenoids of Adenophora triphylla var. japonica rootsC Konno, T Saito, Y Oshima, et al.
The Journal of Organic Chemistry|October 13, 2001
Formation of cyclic ethers via the palladium-catalyzed cycloaddition of activated olefins with allylic carbonates having a hydroxy group at the terminus of the carbon chainM Sekido, K Aoyagi, H Nakamura, et al.
Chemical & Pharmaceutical Bulletin|July 18, 2001
Diels-Alder cycloadditions of 2(1H)-quinolones having an electron-withdrawing group at the 3-position acting as dienophiles with dienesR Fujita, K Watanabe, T Yoshisuji, et al.
Pageof 1