Tadashi Akita - Concepedia

Author

Tadashi Akita

Tokushima University

Also Known As

T AKITA, T Akita, T. AKITA, T. Akita, TADASHI AKITA, Tadashi AKITA, Tadashi Akita, Tadashi. Akita

Publications

770

Citations

H-Index

Concepts

All Affiliations

Tokushima University Kyoto Pharmaceutical University Kyoto University Hiroshima University Sumitomo Dainippon Pharma (Japan)

About

Tadashi Akita is an author at Tokushima University specializing in natural sciences, pharmacology, and biochemistry.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Natural Sciences	12	13	427
2	Biochemistry	11	12	348
3	Medicine	9	9	245
4	Engineering	5	5	219
5	Health Sciences	2	2	24

Tadashi Akita

Publications

581

Citations

H-Index

Page 1

	Year	Citations
Efficient removal of N-benzyloxycarbonyl group by a ‘push–pull’ mechanism using thioanisole–trifluoroacetic acid, exemplified by a synthesis of Met-enkephalin Yoshiaki Kiso, Kazuko Ukawa, Tadashi Akita Journal of the Chemical Society Chemical Communications Chemical EngineeringBioorganic ChemistryThioanisole–trifluoroacetic AcidEngineeringNatural Sciences	1980	79
EDDS-enhanced electrokinetic remediation of heavy metal-contaminated clay soils under neutral pH conditions Tasuma Suzuki, Masakazu NIINAE, Toshiyuki Koga, Colloids and Surfaces A Physicochemical and Engineering Aspects Environmental ElectrochemistryNeutral Ph ConditionsChemical EngineeringEngineeringEnvironmental Engineering	2012	73
Gas chromatography and mass spectrometry of sphingolipid bases. Characterization of sphinga-4,14-dienine from plasma sphingomyelin Alan Polito, Tadashi Akita, Charles C. Sweeley Biochemistry Lipid AnalysisBiological Mass SpectrometryAltmetric Attention ScoreMetabolomic ProfilingGas Chromatography	1968	67
Efficient removal of protecting groups by a 'push-pull' mechanism. II. Deprotection of O-benzyltyrosine with a thioanisole-trifluoroacetic acid system without O-to-C rearrangements. Yoshiaki Kiso, Kazuko Ukawa, Shizuo Nakamura, Chemical and Pharmaceutical Bulletin Bioorganic ChemistryPush-pull MechanismOrganic ChemistryChemistryChemical Biology	1980	64
Deprotection of O-methyltyrosine by a ‘push–pull’ mechanism using the thioanisole–trifluoromethanesulphonic acid system. Application to the convenient synthesis of a potent N-methylenkephalin derivative Yoshiaki Kiso, Shizuo Nakamura, Kaoru Ito, Journal of the Chemical Society Chemical Communications Bioorganic ChemistryPhenolic OxygenOrganic ChemistryClick ChemistryChemistry	1979	42
An ‘active ester’-type mixed anhydride method for peptide synthesis. Use of the new reagent, norborn-5-ene-2,3-dicarboximido diphenyl phosphate (NDPP) Yoshiaki Kiso, Toshitugu Miyazaki, Masahiko Satomi, Journal of the Chemical Society Chemical Communications Inorganic ChemistryChemical EngineeringEngineeringBiochemistryY. Kiso	1980	31
Syntheses of two tyrosine-sulphate containing peptides. Leucosulfakinin (LSK)-II and cholecystokinin (CCK)-12, using the 0--(methylsulphinyl)benzyl serine for the selective sulphation of tyrosine Shiroh Futaki, Takashi Taike, Tadashi Akita, Tetrahedron Bioorganic ChemistryBiochemistryNatural SciencesMedicineSelective Sulphation	1992	27
Use of dimethylformamide–sulphur trioxide complex as a sulphating agent of tyrosine Shiroh Futaki, Takashi Taike, Takeshi Yagami, Journal of the Chemical Society Perkin Transactions 1 BiochemistryNatural SciencesMedicineDimethylformamide–sulphur TrioxideChemical Derivative	1990	26
Efficient deprotection of N<sup>G</sup>-tosylarginine with a thioanisole–trifluoromethanesulphonic acid system Yoshiaki Kiso, Masahiko Satomi, Kazuko Ukawa, Journal of the Chemical Society Chemical Communications Bioorganic ChemistryEngineeringBiochemistryNatural SciencesO-to-c Rearrangement Products	1980	24
Neo‐kyotorphin (Thr—Ser—Lys—Tyr—Arg), a new analgesic peptide Yoshiaki Kiso, Kouki Kitagawa, Nobuyuki Kawai, FEBS Letters	1983	20

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