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Phosphorylation of farnesol by a cell-free system from Botryococcus braunii.
- H. Inoue, T. Korenaga, H. Sagami, T. Koyama, K. Ogura
- Biology, ChemistryBiochemical and biophysical research…
- 30 April 1994
In in vitro experiments with a 10,000 x g supernatant of cell homogenate, squalene was synthesized from farnesyl diphosphate in the presence of NADPH or NADH, but botryococcenes were not synthesized under the same conditions.
Properties of farnesol phosphokinase of Botryococcus braunii
Formation of farnesal and 3-hydroxy-2,3-dihydrofarnesal from farnesol by protoplasts of Botryococcus braunii.
- H. Inoue, T. Korenaga, H. Sagami, T. Koyama, H. Sugiyama, K. Ogura
- ChemistryBiochemical and biophysical research…
- 15 November 1993
Feeding experiments showed that both farnesal and 3-hydroxy-2,3-dihydrofarnesal were efficiently incorporated into botryococcenes, triterpenoid hydrocarbons of the alga.
Synthesis of B-C trans-fused morphine structures. 3. Synthesis of B-C trans-morphine.
Donor-bound glycosylation for various glycosyl acceptors: bidirectional solid-phase semisynthesis of vancomycin and its derivatives.
- T. Doi, A. Kinbara, H. Inoue, Takashi Takahashi
- Chemistry, BiologyChemistry, an Asian journal
- 8 January 2007
Nucleophilic cleavage from the polymer support with acetate, chloride, azido, and thioacetate ions provided vancomycin derivatives in pure form after simple purification.
Synthesis and pharmacology of 5-noralkyl-9beta-methyl-6,7-benzomorphans and stereochemistry of some intermediates.
Compound 18 and the deoxy analog 16 are as potent as morphine and codeine, respectively, as analgetics (mice) and are without physical dependence capacity (monkeys).
Palladium(0)-catalyzed carbonylation on the Multipin™ system