Tsutomu Ishikawa

ORCID: 0000-0003-4516-153X
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About
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Research Areas
  • Chemical synthesis and alkaloids
  • Synthetic Organic Chemistry Methods
  • Chemical Synthesis and Analysis
  • Asymmetric Synthesis and Catalysis
  • Traditional and Medicinal Uses of Annonaceae
  • Plant chemical constituents analysis
  • Synthesis and Catalytic Reactions
  • Oxidative Organic Chemistry Reactions
  • Synthesis of Organic Compounds
  • Synthesis and Biological Evaluation
  • Synthesis and Biological Activity
  • Carbohydrate Chemistry and Synthesis
  • Alkaloids: synthesis and pharmacology
  • Synthesis and Reactions of Organic Compounds
  • Microbial Natural Products and Biosynthesis
  • Bioactive Compounds and Antitumor Agents
  • Berberine and alkaloids research
  • Analytical Chemistry and Chromatography
  • Natural product bioactivities and synthesis
  • Gastric Cancer Management and Outcomes
  • Phytochemical compounds biological activities
  • Chemical Synthesis and Reactions
  • Amino Acid Enzymes and Metabolism
  • Catalytic C–H Functionalization Methods
  • Phytochemistry and Biological Activities

Yamagata University
2023

Waseda University
2023

Nippon Soken (Japan)
2023

The Graduate University for Advanced Studies, SOKENDAI
2023

Nagoya University
2023

Kyushu University
1999-2023

Toneyama National Hospital
2023

Institute of Particle and Nuclear Studies
2023

High Energy Accelerator Research Organization
2023

RIKEN
2023

Guanidine is categorized as an organic superbase, yet its synthetic application immature despite wide potential utility. The role of guanidine in synthesis, including asymmetric reactions, discussed herein.

10.1055/s-2006-926325 article EN Synthesis 2006-01-01

Investigations on modified guanidines, prepared by newly developed methods, as potential chiral auxiliaries led to reasonable asymmetric induction not only in catalytic but also stoichiometric syntheses. These guanidine-mediated reactions may contribute the development of green chemistry because their possible application re-cyclable (economically favored) and easily functionalizable (widely applicable) auxiliaries.

10.1002/1521-3765(20020201)8:3<552::aid-chem552>3.0.co;2-t article EN Chemistry - A European Journal 2002-02-01

Abstract Background and Aim: Colonic perforation is the serious accidental complication. The aim of this study to analyze clinical presentation management recent iatrogenic perforations during therapeutic colonoscopy. Methods: Consecutive patients referred four academic cancer centers in Japan were retrospectively reviewed using each center's endoscopy database medical records. Data was obtained by means an extensive data collection sheet. Since we evaluated including newly developed...

10.1111/j.1440-1746.2007.05022.x article EN Journal of Gastroenterology and Hepatology 2007-06-26

Modified guanidines could effectively mediate asymmetric silylation of secondary alcohols as recyclable bases under simple and mild conditions.

10.1039/b009173l article EN Chemical Communications 2001-01-01

Modified guanidines efficiently catalysed the asymmetric Michael reaction of a prochiral glycine derivative with acrylate or its related compounds either in solution without solvent under simple and mild conditions (>95% ee).

10.1039/b009193f article EN Chemical Communications 2001-01-01

2-Chloro-1,3-dimethylimidazolinium chloride (DMC) (3) can act as a powerful dehydrating agent, replacing DCC (1) under nearly neutral conditions. Its application to acylation and dehydration is described.

10.1021/jo990210y article EN The Journal of Organic Chemistry 1999-08-24

Miroestrol (1) has been isolated previously as an active principle from "Kwao Keur" (Pueraria mirifica), a rejuvenating folk medicine Thailand. Reinvestigation using bioassay-guided purification resulted in the isolation of new potent phytoestrogen, deoxymiroestrol (2). The facile aerial oxidation 2 into 1 suggests possibility that may be artifact.

10.1021/np990547v article EN Journal of Natural Products 2000-01-27

We report 92 patients treated with esophagectomy for superficial esophageal carcinoma (SEC; 9.1% of all resected cancers at our institution). the operative mortality rate was 5.4%. in 24 cases, cancer invasion limited to mucosa, and 68 submucosa. Twenty-three former group had no lymph node involvement, whereas (35.3%) latter metastases. 5-year survival after surgery SEC mucosa 83.5%, which significantly better than that invading submucosa (54.9%). No recurrent disease occurred lesions...

10.1002/1097-0142(19901201)66:11<2319::aid-cncr2820661111>3.0.co;2-1 article EN Cancer 1990-12-01

For large colorectal tumors, the en bloc resection rate achieved by endoscopic mucosal (EMR) is insufficient, and this leads to a high of local recurrence. As submucosal dissection (ESD) has been reported achieve higher lower recurrence in short-term, it expected overcome limitations EMR. We conducted matched case-control study between ESD EMR clarify effectiveness for tumors.Between April 2005 February 2009, total 28 tumors patients were resected followed up colonoscopy at least once....

10.1111/j.1440-1746.2011.06942.x article EN Journal of Gastroenterology and Hepatology 2011-10-17

Three new cyclobutanoid amides with trans-trans-trans configurations, piperarborenine C, D and E, a furanoid lignan, (+)-arborone, together twelve known compounds, were isolated from the stems of Piper arborescens. The structures these compounds determined by means spectral analyses. Piperarborenine (+)-diayangambin, piplartine, piperolactam B, aristolactam BIII, goniothalactam, methyl trans-3,4,5-trimethoxycinnamate possessed anti-platelet aggregation activity in vitro. Among them,...

10.1055/s-2005-864155 article EN Planta Medica 2005-06-01

(−)-Quinine-catalyzed intramolecular oxo-Michael addition (IMA) of 7-hydroxy-5-methoxy-8-tigloylcoumarins was developed for the enantioselective construction 2,3-dimethyl-4-chromanone systems in context asymmetric synthesis anti-HIV-1 active Calophyllum coumarins. Combination IMA and MgI2-assisted demethylation 5-methoxy group along with isomerization formed chromanone as key steps successfully led to concise (+)-inophyllum B (+)-calanolide A, possible candidates AIDS drugs. Further...

10.1021/jo035753t article EN The Journal of Organic Chemistry 2004-03-12

2-Chloro-1,3-dimethylimidazolinium chloride (DMC) (1) can act as a powerful dehydrating equivalent to DCC (2) under nearly neutral conditions. Its application the construction of heterocycles through dehydration reactions is described.

10.1021/jo9909756 article EN The Journal of Organic Chemistry 1999-08-24

Abstract Of 393 patients with squamous‐cell carcinoma in the thoracic esophagus, 60 were found by histologic examination to have intramural metastasis. Metastases 50 of these identified gross inspection. There appeared be no preference for location proximal primary lesion. Eighteen had metastasis gastric wall, which suggested existence communicating lymphatic channels between wall esophagus and stomach. All tumors invaded beyond submucosa. These (group A) compared a group matched control...

10.1002/ijc.2910500111 article EN International Journal of Cancer 1992-01-02

Bioassay-guided fractionation of the root wood Zanthoxylum wutaiense led to isolation 11 new compounds, wutaiensol methyl ether (1), demethoxywutaiensol (2), wutaiensate (3), 7-hydroxyanodendroate (4), 7-methoxyanodendroate (5), wutaifuranol (6), 7-methoxywutaifuranol (7), 7-methoxywutaifuranal (8), wutaifuranate (9), 7-methoxybenzofuran-5-carboxylate (10), and wutaipyranol (12), together with another 37 known which one, 7-methoxybenzofuran-5-carboxaldehyde (11), was not previously as a...

10.1021/np700719e article EN Journal of Natural Products 2008-06-20

Abstract The guanidine‐catalyzed 6‐ exo ‐ trig ‐type intramolecular asymmetric oxa‐Michael addition of α,β‐unsaturated esters with a 2‐hydroxyaryl moiety at the C‐5 carbon has been examined for construction chromane skeletons quaternary chiral center. bulkiness alkyl group and E / Z geometry ester function played important roles in induction (4 S ,5 )‐2‐[( R )‐1‐hydroxymethyl‐2‐phenylethylimino]‐1,3‐dimethylimidazolidine (or its enantiomer) carrying aryl pendants 4‐ 5‐positions was found to...

10.1002/ejoc.200800089 article EN European Journal of Organic Chemistry 2008-04-11

There are a number of reports indicating that <i>CYP2B6</i>*<i>6</i> (c.516G&gt;T and c.785A&gt;G) is responsible for decreased clearance efavirenz (EFV), although increased disposition cyclophosphamide (CPA) in individuals with this polymorphism was observed. Thus, we hypothesized the effects two single nucleotide polymorphisms (SNPs) on metabolism drugs might be considerably different between these agents. To clarify possibility, expressed major variants enzyme, CYP2B6.6 (Q172H K262R)...

10.1124/dmd.111.039586 article EN Drug Metabolism and Disposition 2011-08-05
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