S. Harusawa

发表

Synthesis of two estradiol-imidazole C-ribonucleoside hybrid compounds exhibiting inhibitory effects against type 1 17β-hydroxysteroid dehydrogenase

M. Sakaguchi, S. Harusawa, C. Kojima, 2010 .

Efficient Approaches to S-alkyl-N-alkylisothioureas and Application to Novel Histamine H3R Antagonists.

A. Yamatodani, S. Harusawa, Hiroki Yoneyama, 2016, Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan.

Diethyl phosphorocyanidate (DEPC): a versatile reagent for organic synthesis

S. Harusawa, T. Shioiri, T. Shioiri*, 2016 .

Intracerebroventricular administration of histamine H3 receptor antagonists decreases seizures in rat models of epilepsia.

S. Harusawa, Y. Fujii, C. Harada, 2004, Methods and findings in experimental and clinical pharmacology.

Design and synthesis of an aminobenzo-15-crown-5-labeled estradiol tethered with disulfide linkage

S. Harusawa, C. Kojima, Lisa Araki, 2004 .

Histamine H3 receptor antagonist OUP-186 attenuates the proliferation of cultured human breast cancer cell lines.

M. Sakaguchi, S. Harusawa, Y. Usami, 2016, Biochemical and biophysical research communications.

C4-Alkylamination of C4-Halo-1H-1-tritylpyrazoles Using Pd(dba)2 or CuI

S. Harusawa, Y. Usami, Hiroki Yoneyama, 2020, Molecules.

Introduction of Fluorine into Antitumor-Active Dinuclear Platinum(II) Complexes Leads to Modulation of In Vivo Antitumor Activity in Mice.

K. Hiramoto, S. Harusawa, Hiroki Yoneyama, 2022, Inorganic chemistry.

Synthesis of novel 4(5)-(5-aminotetrahydropyran-2-yl)imidazole derivatives and their in vivo release of neuronal histamine measured by brain microdialysis.

A. Yamatodani, S. Harusawa, Lisa Araki, 2007, Chemical & pharmaceutical bulletin.

Syntheses and Glycosidase Inhibitory Activities, and in Silico Docking Studies of Pericosine E Analogs Methoxy-Substituted at C6

Y. Uesawa, S. Harusawa, Y. Usami, 2020, Marine drugs.

A synthesis of taxusin

S. Harusawa, R. Lowenthal, R. Juo, 1988 .

Synthesis of fluorinated isoxazoles using Selectfluor™: preparation and characterization of 4-fluoroisoxazole, 4,4,5-trifluoroisoxazoline and 4,4-difluoro-5-hydroxyisoxazoline systems from one-pot and multi-step processes

D. Yufit, G. Sandford, S. Harusawa, 2016 .

Synthesis of 4(5)-(a-D-Xylofuranosyl)imidazole Starting from L-Arabinose: Mitsunobu Cyclization via C4’-Oxyphosphonium Intermediate

S. Harusawa, Lisa Araki, T. Kurihara, 2001 .

Synthesis of 6-Halo-Substituted Pericosine A and an Evaluation of Their Antitumor and Antiglycosidase Activities

Mizuki Morita, S. Harusawa, Y. Usami, 2022, Marine drugs.

CYANO PHOSPHATE : AN EFFICIENT INTERMEDIATE FOR THE CHEMOSELECTIVE CONVERSION OF CARBONYL COMPOUNDS TO NITRILES

S. Harusawa, T. Kurihara, R. Yoneda, 1991 .

Diethyl phosphorocyanidated (DEPC). A novel reagent for the classical Strecker's α-amino nitrile synthesis☆

S. Harusawa, Y. Hamada, T. Shioiri, 1979 .

Application of Cyanohydrin Ο-Diethyl Phosphates in Organic Synthesis

S. Harusawa, T. Kurihara, R. Yoneda, 1988 .

NEW METHODS AND REAGENTS IN ORGANIC SYNTHESIS. 5. DIETHYL PHOSPHOROCYANIDATE (DEPC). A NOVEL REAGENT FOR THE CLASSICAL STRECKER′S α-AMINO NITRILE SYNTHESIS

S. Harusawa, Y. Hamada, T. Shioiri, 1980 .

NEW METHODS AND REAGENTS IN ORGANIC SYNTHESIS. PART 12. REACTION OF DIETHYLPHOSPHOROCYANIDATE (DEPC) WITH AROMATIC AMINE OXIDES. A MODIFIED REISSERT-HENZE-REACTION

S. Harusawa, Y. Hamada, T. Shioiri, 1981 .

Synthesis of novel tetrazole C5-linked C0- and C2-ribonucleoside phosphoramidites using MePOM and POM groups for probing RNA catalysis

D. Lilley, T. J. Wilson, S. McPhee, 2012 .

CuI-Catalyzed Coupling Reactions of 4-Iodopyrazoles and Alcohols: Application toward Withasomnine and Homologs

K. Nishikawa, S. Harusawa, Y. Usami, 2021, Molecules.

Synthesis of Dihydrooxepino[3,2-c]Pyrazoles via Claisen Rearrangement and Ring-Closing Metathesis from 4-Allyloxy-1H-pyrazoles

S. Harusawa, Y. Usami, Hiroki Yoneyama, 2018, Molecules.

Transformation of Carbonyl Compounds into Homologous Alkynes under Neutral Conditions: Fragmentation of Tetrazoles Derived from Cyanophosphates.

M. Numata, S. Harusawa, Y. Usami, 2017, The Journal of organic chemistry.

Synthesis of five-membered unsaturated compounds from ketones via cyanophosphates under neutral conditions: [1,5]-CH insertion of alkylidene carbenes generated by tetrazole fragmentation

S. Harusawa, Y. Usami, Hiroki Yoneyama, 2017 .

Development of New Synthetic Reactions Using Hetero-Heavy Atoms and Their Application to Synthesis of Biofunctional Molecules.

S. Harusawa, 2020, Chemical & pharmaceutical bulletin.

Divergent synthesis and evaluation of inhibitory activities against cyclooxygenases-1 and -2 of natural withasomnines and analogues.

S. Harusawa, Y. Usami, R. Watanabe, 2012, Chemical & pharmaceutical bulletin.

A simple one-pot synthesis of silylated and acylated cyanohydrins

S. Harusawa, T. Kurihara, R. Yoneda, 1986 .

Synthesis and structure-activity relationships of tetrazolato-bridged dinuclear platinum(II) complexes: A small modification at tetrazole C5 markedly influences the in vivo antitumor efficacy.

K. Hiramoto, T. Tsuchiya, S. Harusawa, 2019, Journal of inorganic biochemistry.

Specific Conformational Change in Giant DNA Caused by Anticancer Tetrazolato-Bridged Dinuclear Platinum(II) Complexes: Middle-Length Alkyl Substituents Exhibit Minimum Effect.

K. Yoshikawa, T. Imanaka, Wakao Fukuda, 2017, Inorganic chemistry.

Efficient Transformation of Inactive Nitriles into 5-Substituted 1H-Tetrazoles Using Microwave Irradiation and Their Applications

S. Harusawa, Y. Usami, Hiroki Yoneyama, 2013, Synthesis.

Meisenheimer rearrangement of azetopyridoindoles, VI. Synthesis of 12-carbaeudistomin and related compounds.

H. Matsumoto, S. Harusawa, T. Kurihara, 1994, Chemical & pharmaceutical bulletin.

Synthesis of Dihydropyrano[3,2-c]pyrazoles via Double Bond Migration and Ring-Closing Metathesis

S. Harusawa, Y. Usami, Hiroki Yoneyama, 2019, Molecules.

An Abnormal Reaction of N-tert-Butoxycarbonyl Group: Mechanistic Consideration for the Preparation of 2-Oxotetrahydro-1,3-oxazine

S. Harusawa, T. Kurihara, Y. Matsubara, 1988 .

Cyanophosphate: An efficient intermediate for conversion of carbonyl compounds to nitriles

S. Harusawa, T. Kurihara, R. Yoneda, 1989 .

A novel synthesis of α,β-unsaturated nitriles from aromatic ketones via cyanophosphates

S. Harusawa, Y. Hamada, T. Shioiri, 1984 .

Dephosphorylation of cyano diethyl phosphates by reduction with lithium–liquid ammonia: an efficient method for conversion of carbonyl compounds into nitriles

S. Harusawa, T. Kurihara, Takahiro Osaki, 1990 .

Synthesis of Natural O-Linked Carba-Disaccharides, (+)- and (−)-Pericosine E, and Their Analogues as α-Glucosidase Inhibitors

S. Harusawa, Y. Usami, Hiroki Yoneyama, 2017, Marine drugs.

Enantiomeric composition of natural pericosine A derived from Periconia byssoides and α-glycosidase inhibitory activity of (-)-enantiomer.

S. Harusawa, Y. Usami, Hiroki Yoneyama, 2022, Chirality.

Synthesis of Imidazole C1- and C3-Ribonucleoside Phosphoramidites for Probing Catalytic Mechanism in Ribozyme

D. Lilley, S. Harusawa, Kensuke Fujii, 2011 .

Synthesis of 4(5)-(5'-Amino-5'-deoxy-a-L-arabinofuranosyl)imidazole and Its 5'-Derivatives Using Modified Mitsunobu Cyclization: Synthetic Studies toward Novel Histamine H3-Ligands

S. Harusawa, Lisa Araki, Hirokazu Suzuki, 2000 .

Stereoselective synthesis of the C-4 linked imidazole nucleosides using modified Mitsunobu reaction

S. Harusawa, H. Ohishi, T. Kurihara, 1995 .

Application of Cyanophosphates in Organic Synthesis. Reactivity of α-Cyano-α-diethylphosphonooxy Anions

S. Harusawa, T. Kurihara, R. Yoneda, 1987 .

Non-aqueous cyanation of halides using lithium cyanide

S. Harusawa, T. Kurihara, Y. Omori, 1987 .

Meisenheimer Rearrangement of 2-Ethyl-1,4,5,10b-tetrahydro-2H-azetopyrido[3,4-b]indole N-Oxides. Formation of 3,6-Epoxy-1,2,3,4,5,6-hexahydroazocino[5,6-b]indoles

S. Harusawa, T. Kurihara, R. Yoneda, 1991 .

Synthetic Challenges in the Construction of 8- to 10-Membered Pyrazole-Fused Rings via Ring-Closing Metathesis

S. Harusawa, Y. Usami, Hiroki Yoneyama, 2020 .

MICROWAVE-AIDED ONE-POT DEHYDRATION OF THE ALCOHOL DERIVED FROM (-)-SHIKIMIC ACID FOR EFFICIENT SYNTHESIS OF PERICOSINES

S. Harusawa, Y. Usami, Hiroki Yoneyama, 2014 .

Synthesis of marine natural product (-)-pericosine E.

N. Murata, S. Harusawa, Y. Usami, 2014, Organic letters.

A New Synthesis of Some Non-Steroidal Anti-Inflammatory Agents via Cyanophosphates1)

Shuji Nakamura, S. Harusawa, Y. Hamada, 1984 .

[3,3]Sigmatropic ring expansion of cyclic thionocarbonates. 8. highly stereoselective synthesis of (Z- or (E)-double bonds by controlling chairlike-boatlike transition states in the [3,3]sigmatropic rearrangement of 8-membered thionocarbonates

S. Harusawa, T. Kurihara, R. Yoneda, 1992 .

Efficient Synthesis of a 5α-Reductase Inhibitor, 3-(Tetrazol-5-yl)-3,5-pregnadien-20-one through Allylic Rearrangement of Cyanophosphates

S. Harusawa, Y. Usami, Hiroki Yoneyama, 2019, Synthesis.

New Methods and Reagents in Organic Synthesis. Part 45. A New Synthesis of Some Non-Steroidal Antiinflammatory Agents via Cyanophosphates.

S. Harusawa, Y. Hamada, T. Kurihara, 1986 .

CYANOPHOSPHORYLATION OF KETONES AND ALDEHYDES USING DIETHYL PHOSPHOROCYANIDATE (DEPC)

S. Harusawa, Y. Hamada, T. Shioiri, 1983 .

New methods and reagents in organic synthesis, 23, diethyl phosphorocyanidate(DEPC): a useful reagent for an unprecedented transformation of sulfinic acids to thiocyanates

S. Harusawa, T. Shiori, 1982 .

New methods and reagents in organic synthesis. XIII. Structure of 3β-(1-pyrrolidinyl)-5α-cholestane-3α-carbonitrile

T. Ishida, S. Harusawa, M. Inoue, 1981 .

In Vitro Cytotoxicity and In Vivo Antitumor Efficacy of Tetrazolato-Bridged Dinuclear Platinum(II) Complexes with a Bulky Substituent at Tetrazole C5

K. Hiramoto, S. Harusawa, Hiroki Yoneyama, 2019, Inorganics.

Efficient and beta-Stereoselective Synthesis of 4(5)-(beta-D-Ribofuranosyl)- and 4(5)-(2-Deoxyribofuranosyl)imidazoles(1).

S. Harusawa, H. Ohishi, T. Kurihara, 1996, The Journal of organic chemistry.

[Synthetic studies of imidazole C-nucleosides toward biofunctional molecules].

S. Harusawa, Lisa Araki, 2010, Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan.

Efficient and β-Stereoselective Synthesis of 4(5)-(β-D-Ribofuranosyl)- and 4(5)-(2-Deoxyribofuranosyl)imidazoles.

S. Harusawa, H. Ohishi, H. Moriyama, 2010 .

Mass determination of phosphoramidites.

D. Lilley, S. Harusawa, T. Kurihara, 2006, Current protocols in nucleic acid chemistry.

Nucleobase catalysis in the hairpin ribozyme.

D. Lilley, T. J. Wilson, J. Ouellet, 2006, RNA.

Synthesis of novel C4-linked imidazole ribonucleoside phosphoramidites for probing general acid and base catalysis in ribozyme

D. Lilley, S. Harusawa, Lisa Araki, 2005 .

Accurate molecular weight measurements of nucleoside phosphoramidites: a suitable matrix of mass spectrometry

D. Lilley, S. Harusawa, Lisa Araki, 2005 .

Synthesis of C4-linked imidazole ribonucleoside phosphoramidite with pivaloyloxymethyl (POM) group

D. Lilley, S. Harusawa, Lisa Araki, 2004 .

Efficient synthesis of trans- or cis-4(5)-(5-aminomethyltetrahydrofuran-2-yl)imidazoles via diazafulvene intermediates: synthetic approach toward human histamine H4)-ligands.

A. Yamatodani, S. Harusawa, Lisa Araki, 2003, Chemical & pharmaceutical bulletin.

Synthesis of (+/-)-trans- or cis-(5-aminomethyltetrahydrofuranyl)imidazole by Mitsunobu cyclization: synthetic studies toward novel histamine H3 or H4-ligands.

S. Harusawa, Lisa Araki, H. Ohishi, 2003, Chemical & pharmaceutical bulletin.

Synthesis of imifuramine and its stereoisomers exhibiting histamine H3-agonistic activity

A. Yamatodani, S. Harusawa, Lisa Araki, 1999 .

Synthesis and evaluation of N-alkyl-S-[3-(piperidin-1-yl)propyl]isothioureas: high affinity and human/rat species-selective histamine H(3) receptor antagonists.

Hiroki Yoneyama, Kouichi Yamamoto, Koichi Sawada, 2013, Bioorganic & medicinal chemistry letters.

Efficient and β-Stereoselective Synthesis of 4(5)-Methyl-5(4)-(5-amino-5-deoxy-β-D-ribofuranosyl)imidazole and Related Compounds Exhibiting Antiulcer Activity

S. Harusawa, H. Ohishi, T. Kurihara, 1997 .

Synthesis of C4-Linked C0- and C2-Imidazole 2′-Deoxyribonucleoside Phosphoramidites and Imidazole Base-Pairing Effects on DNA

S. Harusawa, Y. Usami, Hiroki Yoneyama, 2014, Synthesis.

Nucleobase participation in ribozyme catalysis.

D. Lilley, S. Harusawa, Lisa Araki, 2005, Journal of the American Chemical Society.

Syntheses of cyclopentyl nucleoside (−)-neplanocin A through tetrazole-fragmentation from cyanophosphates

S. Harusawa, Y. Usami, Hiroki Yoneyama, 2018 .

Synthesis of Triazol Cn-Ribonucleoside Phosphoramidites Using β-Ribofuranosyl-Cn-acetylenes for RNA Catalysis Probing

S. Harusawa, Y. Usami, Hiroki Yoneyama, 2018 .

Efficient synthesis of 2'-O-cyanoethylated imidazole C-ribonucleoside phosphoramidite: a practical building block for probing the catalytic mechanism of ribozymes

D. Lilley, S. Harusawa, Lisa Araki, 2010 .

Synthetic Studies of Imidazole C-Nucleosides Toward Biofunctional Molecules

S. Harusawa, Lisa Araki, 2011 .

Synthesis of novel C4-linked C2-imidazole ribonucleoside phosphoramidite and its application to probing the catalytic mechanism of a ribozyme.

D. Lilley, T. J. Wilson, S. Harusawa, 2009, The Journal of organic chemistry.

A selective human H(4)-receptor agonist: (-)-2-cyano-1-methyl-3-[(2R,5R)-5- [1H-imidazol-4(5)-yl]tetrahydrofuran-2-y] methylguanidine.

Rob Leurs, Takeshi Hashimoto, O. Zuiderveld, 2003, Journal of medicinal chemistry.

Synthesis of 4(5)-[5-(Aminomethyl)tetrahydrofuran-2-yl- or 5-(Aminomethyl)-2,5-dihydrofuran-2-yl]imidazoles by Efficient Use of a PhSe Group: Application to Novel Histamine H3-Ligands1

A. Yamatodani, S. Harusawa, Lisa Araki, 1999 .

Synthetic Studies of Imidazole C-Nucleoside Derivatives : Their Application to Histamine H3- and H4-Ligands

S. Harusawa, Lisa Araki, T. Kurihara, 2003 .

Efficient Synthesis of trans‐ or cis‐4(5)‐(5‐Aminomethyltetrahydrofuran‐2‐yl)imidazoles via Diazafulvene Intermediates: Synthetic Approach Toward Human Histamine H4‐Ligands.

A. Yamatodani, S. Harusawa, Lisa Araki, 2003 .

Synthesis of (.+-.)-trans- or cis-(5-Aminomethyltetrahydrofuranyl)imidazole by Mitsunobu Cyclization: Synthetic Studies Toward Novel Histamine H3 or H4-Ligands.

S. Harusawa, Lisa Araki, H. Ohishi, 2003 .

RNA folding and the origins of catalytic activity in the hairpin ribozyme.

D. Lilley, T. Ha, T. J. Wilson, 2007, Blood cells, molecules & diseases.

Efficient and β-Stereoselective Synthesis of 4(5)-Methyl-5(4)-(5- amino-5-deoxy-β-D-ribofuranosyl)imidazole and Related Compounds Exhibiting Antiulcer Activity.

S. Harusawa, H. Ohishi, T. Kurihara, 1997 .

Efficient Synthesis of 2′‐O‐Cyanoethylated Imidazole C‐Ribonucleoside Phosphoramidite: A Practical Building Block for Probing the Catalytic Mechanism of Ribozymes.

D. Lilley, S. Harusawa, Lisa Araki, 2010 .

Transformation of γ-ketoaldehyde acetals into 3-substituted-2-cyclopentenones via cyanophosphates under mild conditions

S. Harusawa, Y. Usami, Hiroki Yoneyama, 2021 .

A novel synthetic method of 2,4-disubstituted oxazoles using carboxylic acid-derived Bu2Sn[OC(O)R]2

S. Harusawa, Y. Usami, Hiroki Yoneyama, 2020 .

Synthetic Studies of Imidazole C‐Nucleoside Derivatives: Their Application to Histamine H3‐ and H4‐Ligands

S. Harusawa, Lisa Araki, T. Kurihara, 2003 .

TMSN3-Bu2Sn(OAc)2: A modified and mild reagent system for Wittenberger tetrazole-synthesis

S. Harusawa, Y. Usami, Hiroki Yoneyama, 2020 .

Tetrazole-Fragmentation for the Generation of Alkylidene Carbenes from Cyanophosphates under Neutral Conditions and Its Application to Organic Synthesis

S. Harusawa, Hiroki Yoneyama, 2018 .

Synthesis of C-nor-4,6-secocamptothecin and related compounds

S. Harusawa, T. Kurihara, R. Yoneda, 1993 .

A New Synthesis of Polysubstituted Cyclopropanes

S. Harusawa, T. Kurihara, R. Yoneda, 1987 .

Synthesis of an indole analog of magallanesine via the [1,2]‐meisenheimer rearrangement

S. Harusawa, Tetsuya Kimura, T. Kurihara, 1996 .

[3,3]sigmatropic ring expansion of cyclic thionocarbonates. 13.1 synthesis of medium-membered heterocyclic allenes and synthetic application to antifungal constitutent of Sapium japonicum

S. Harusawa, H. Ohishi, T. Kurihara, 1995 .

(3,3)Sigmatropic Ring Expansion of Cyclic Thionocarbonates. Part 13. Synthesis of Medium-Membered Heterocyclic Allenes and Synthetic Application to Antifungal Constituent of Sapium japonicum.

S. Harusawa, H. Ohishi, T. Kurihara, 1995 .

[3, 3] Sigmatropic Ring Expansion of Cyclic Thionocarbonates of Medium Ring-Size

S. Harusawa, T. Kurihara, 1995 .

[3,3]Sigmatropic ring expansion of cyclic thionocarbonates. 12. synthesis of (−)-yellow scale pheromone☆

S. Harusawa, T. Kurihara, R. Yoneda, 1993 .

[3,3]sigmatropic ring expansion of cyclic thionocarbonates. VII: On the formation of 8-membered thionocarbonates as the intermediates

S. Harusawa, H. Ohishi, Ryouji Yoneda, 1992 .

[3, 3]Sigmatropic Ring Expansion of Cyclic Thionocarbonates. IV. Relatioship between Ring Size of Cyclic Thionocarbonates and Geometry of Created Double Bond in Medium- and Large-Membered Thiolcarbonates

S. Harusawa, T. Kurihara, T. Kurokawa, 1991 .

[3,3]sigmatropic ring expansion of cyclic thionocarbonates.3. Computational evaluation of the transition states

S. Harusawa, H. Ohishi, T. Kurihara, 1991 .

(3,3)Sigmatropic Ring Expansion of Cyclic Thionocarbonates of Medium Ring-Size

S. Harusawa, T. Kurihara, 1996 .

Highly stereoselective synthesis of (Z)- or (E)-double bonds with conformational control in [3,3]sigmatropic ring expansion of 8-membered thionocarbonates

S. Harusawa, T. Kurihara, R. Yoneda, 1990 .

[3,3]Sigmatropic ring expansion of cyclic thionocarbonates. 9. total synthesis of (±)-yellow scale pheromone via 10-membered thiolcarbonate

S. Harusawa, T. Kurihara, R. Yoneda, 1993 .

[3,3]Sigmatropic ring expansion of cyclic thionocarbonates. 5. Stereoselective synthesis of the yellow scale pheromone

S. Harusawa, T. Kurihara, R. Yoneda, 1992 .

(3,3)Sigmatropic Ring Expansion of Cyclic Thionocarbonates. Part 12. Synthesis of (-)-Yellow Scale Pheromone (IX).

S. Harusawa, T. Kurihara, R. Yoneda, 1994 .

Synthesis of medium-membered heterocyclic allenes by [3,3]sigmatropic rearrangement and its synthetic application to the antifungal constituent of sapium japonicum

S. Harusawa, T. Kurihara, R. Yoneda, 1994 .

(3,3)Sigmatropic Ring Expansion of Cyclic Thionocarbonates. Part 7. On the Formation of 8-Membered Thionocarbonates as the Intermediates.

S. Harusawa, H. Ohishi, T. Kurihara, 1993 .

A total synthesis of magallanesine via [1, 2]-Meisenheimer rearrangement

S. Harusawa, T. Kurihara, Y. Sakamoto, 1994 .

AN EFFICIENT SYNTHESIS OF MAGALLANESINE USING 1,2-MEISENHEIMER REARRANGEMENT AND HECK CYCLIZATION

S. Harusawa, T. Kurihara, Y. Sakamoto, 1996 .

Heck-Mizoroki reaction of 4-iodo-1H-pyrazoles

S. Harusawa, Y. Usami, H. Ichikawa, 2011 .

Allylic Rearrangement of Cyanophosphates. III. : Reaction of Acyclic Enone Cyanophosphates

S. Harusawa, T. Kurihara, R. Yoneda, 1986 .

An efficient and convenient synthesis of 4-vinylimidazoles using a novel Horner-Wadsworth-Emmons (HWE) reagent: Synthetic studies toward novel histamine H3-Ligands

S. Harusawa, Lisa Araki, T. Kurihara, 2002 .

An Efficient and Convenient Synthesis of 4‐Vinylimidazoles Using a Novel Horner—Wadsworth—Emmons (HWE) Reagent: Synthetic Studies Toward Novel Histamine H3‐Ligands.

S. Harusawa, Lisa Araki, T. Kurihara, 2002 .

Synthesis of 5-(4-Pyrazolyl and 4-Isoxazolyl)-1,3-dihydro-2H-1,4-benzodiazepin-2-ones

S. Harusawa, T. Kurihara, Yutaka Nakamura, 1989 .

Synthesis of 5-(4-Pyrazolyl and 4-Isoxazolyl)-1,3-dihydro-2H-1,4-benzodiazepin-2-ones.

S. Harusawa, T. Kurihara, Yutaka Nakamura, 1990 .

Recyclization of 2-oxotetrahydro-1,3-oxazines accompanied by decarboxylation: a convenient synthesis of tetrahydropyridine, quinolizidine, and indolizidine skeletons

S. Harusawa, T. Kurihara, Y. Matsubara, 1988 .

Synthesis and cycloaddition reaction of 2-cyano-3-indoleacetonitriles

S. Harusawa, T. Kurihara, M. Hanakawa, 1986 .

Reaction of 3-acylindoles with diethyl phosphorocyanidate. A facile synthesis of 2-cyano-3-indoleacetonitriles

S. Harusawa, T. Kurihara, M. Hanakawa, 1985 .

Synthesis and Cycloaddition Reaction of 2-Cyano-3-indoleacetonitriles.

S. Harusawa, T. Kurihara, M. Hanakawa, 1987 .

[3, 3]Sigmatropic Ring Expansion of Cyclic Thionocarbonates. VI. Regioselective Wohl-Ziegler Bromination of 10-Membered Thiolcarbonates

S. Harusawa, H. Ohishi, T. Kurihara, 1992 .

(3,3)Sigmatropic Ring Expansion of Cyclic Thionocarbonates. Part 6. Regioselective Wohl‐Ziegler Bromination of 10‐Membered Thiolcarbonates.

S. Harusawa, H. Ohishi, T. Kurihara, 1993 .

Regiospecific arylation of 1,4-benzoquinone cyanohydrin phosphate: synthesis of 3-aryl-4-hydroxybenzonitriles

S. Harusawa, T. Kurihara, J. Hirai, 1987 .