H. Katayama

发表

Secondary joining of the bile ducts during the hepatogenesis of the mouse embryo

N. Shiojiri, H. Katayama, 2004, Anatomy and Embryology.

Development of Dolichos biflorus agglutinin (DBA) binding sites in the bile duct of the embryonic mouse liver

N. Shiojiri, H. Katayama, 2004, Anatomy and Embryology.

Oridonin, a new diterpenoid from Isodon species

E. Fujita, T. Fujita, M. Shibuya, 1967 .

Pyrimidine Derivatives; 1. The Highly Regioselective 4-Thionation of Pyrimidine-2,4(1H,3H)-dione Derivatives with Lawesson Reagent

K. Kaneko, T. Wakabayashi, H. Katayama, 1988 .

Intramolecular aromatic amination by a hydrazino group for the synthesis of indolo[1,2-b]indazole derivatives

Yong‐Ming Zhu, H. Katayama, Y. Kiryu, 2002 .

Preparation and bioactivity of pyrazole derivatives as potential cross-linking agent

H. Katayama, T. Oshiyama, 1997 .

Synthesis of pyrazolo[1,5-a]indoles via copper(I)-catalyzed intramolecular amination

S. Ji, Liena Qin, Yong‐Ming Zhu, 2007 .

Synthesis of 2-Aryl-2H-indazoles via Copper(I)-Catalyzed Intramolecular Amination Reaction

S. Ji, Liena Qin, Yong‐Ming Zhu, 2007 .

The total synthesis of (+)-ryanodol. Part III. Preparation of (+)-anhydroryanodol from a key pentacyclic intermediate

A. Bélanger, C. Liao, J. Maffrand, 1990 .

The total synthesis of (+)-ryanodol. Part I. General strategy and search for a convenient diene for the construction of a key tricyclic intermediate

A. Bélanger, C. Liao, J. Maffrand, 1990 .

The total synthesis of (+)-ryanodol. Part II. Model studies for rings B and C of (+)-anhydroryanodol. Preparation of a key pentacyclic intermediate

A. Bélanger, C. Liao, J. Maffrand, 1990 .

The total synthesis of (+)-ryanodol. Part IV. Preparation of (+)-ryanodol from (+)-anhydroryanodol

A. Bélanger, C. Liao, J. Maffrand, 1990 .

Total synthesis of ryanodol

A. Bélanger, C. Liao, J. Maffrand, 1979 .

Copper(I)-Catalyzed Tandem Cyclization/Condensation Reaction to Novel 4,5-Dihydropyrazolo[1,5-a]quinolines and Pyrazolo[1,5-a]indoles

C. Hang, H. Katayama, Yongming Zhu, 2011 .

REACTION OF 1-AZABICYCLO[1.1.0]BUTANE WITH ACTIVATED AMIDES

Y. Nagao, S. Sano, K. Hayashi, 2009 .

Synthetic inhibitors of DNA topoisomerase I and II.

K. Kaneko, N. Takatsu, Y. Kawada, 1999, Chemical & pharmaceutical bulletin.

Intramolecular reaction of the hydrazonyl group with formyl and oxo groups: preparation of pyrazolo[1,5-a]indoles and related pyrazolo compounds

N. Takatsu, Jing-Kang Shen, H. Katayama, 1993 .

Preparation and Bioactivity of Pyrazole Derivatives as Potential Cross- Linking Agents.

H. Katayama, T. Oshiyama, 1997 .

Effects of magnesium salts and amines on the stereoselectivity in the imine aldol reaction.

K. Hayashi, Y. Nagao, S. Sano, 2007, Chemical & pharmaceutical bulletin.

Amino-Claisen Rearrangement. I

H. Katayama, 1978 .

Amino-Claisen rearrangement. III. The effects of alkyl substituents on the allyl group upon the rearrangement.

N. Takatsu, A. Kato, H. Katayama, 1983 .

Proximity Effects in Acid and Base‐Catalysed Ether Formation

C. A. Grob, H. Katayama, 1977 .

Synthesis of Indolo[1,2-b]indazole Derivatives via Copper(I)-Catalyzed Intramolecular Amination Reaction

Yong‐Ming Zhu, C. Hang, H. Katayama, 2010 .

Synthesis of Pyrazolo[1,5-a]indoles via Copper(I)-Catalyzed Intramolecular Amination.

S. Ji, Liena Qin, Yong‐Ming Zhu, 2007 .

Synthesis of Indolo[1,2‐b]indazole Derivatives.

K. Kaneko, O. Kato, N. Takatsu, 2004 .

Synthesis of indolo[1,2-B]indazole derivatives

K. Kaneko, O. Kato, N. Takatsu, 2003 .

Inhibition of DNA topoisomerases II and/or I by pyrazolo[1,5-a]indole derivatives and their growth inhibitory activities.

T. Andoh, T. Yamori, K. Umemura, 2002, Molecular pharmacology.

Anti-cancer activities of pyrazolo[1,5-a]indole derivatives.

K. Kaneko, H. Katayama, Y. Kiryu, 2000, Chemical & pharmaceutical bulletin.

Heterocyclic analogues of quinone methide: preparation and cytotoxicity of 3-oxo-3H-pyrazolo[1,5-a]indole derivatives.

N. Tagawa, K. Kaneko, Y. Ikeda, 1997, Chemical & pharmaceutical bulletin.

Terpenoids—XIV : Formal chemical conversion of enmein into ent-kaurene, atisine, garryine and veatchine

E. Fujita, T. Fujita, H. Katayama, 1970 .

Synthesis and reaction of 1-azabicyclo[3.1.0]hexane.

K. Hayashi, Y. Nagao, S. Sano, 2009, Chemical & pharmaceutical bulletin.

Repair of DNA damage in a mitochondrial lysate of Xenopus laevis oocytes.

A. Matsuda, M. Ryoji, H. Katayama, 1996, Nucleic acids research.

Terpenoids. XXIV. Isolation of Isodonal and Epinodosin from Isodon japonicus and Structure Elucidation of Sodoponin and Epinodosinol, Novel Diterpenoids of the Same Plant

E. Fujita, T. Fujita, M. Shibuya, 1973 .

Terpenoids. Part XV. Structure and Absolute Configuration of Oridonin isolated from Isodon japonicus and Isodon trichocarpus

E. Fujita, T. Fujita, M. Shibuya, 1970 .

Amino-Claisen Rearrangement. IV. Quaternary Amino-Claisen Rearrangement of N-Allyljulolidinium Derivatives

K. Kaneko, H. Katayama, M. Ohkoshi, 1984 .

The chemical conversion of enmein into -15-kaurene and -16-kaurene

Y. Nagao, E. Fujita, T. Fujita, 1969 .

AMINO‐CLAISEN REARRANGEMENT. IV. QUATERNARY AMINO‐CLAISEN REARRANGEMENT OF N‐ALLYLJULOLIDINIUM DERIVATIVES

K. Kaneko, H. Katayama, M. Ohkoshi, 1984 .

The Total Synthesis of (+)-Ryanodol. Part 1. General Strategy and Search for a Convenient Diene for the Construction of a Key Tricyclic Intermediate.

A. Bélanger, C. Liao, J. Maffrand, 1990 .

TWO TYPES OF INDIRECT CYCLODIMERIZATION OF BIACETYL VIA ITS ENOL SILYL ETHERS

I. Ryu, S. Murai, K. Kondo, 1977 .

SYNTHESIS VIA SILYL ALKENYL ETHERS. PART XI. TWO TYPES OF INDIRECT CYCLODIMERIZATION OF BIACETYL VIA ITS ENOL SILYL ETHERS

I. Ryu, S. Murai, K. Kondo, 1978 .

Amino-Claisen Rearrangement. II. Quaternary Amino-Claisen Rearrangement of Anilinium Compounds with ortho Substituents

N. Takatsu, H. Katayama, 1981 .

Terpenoids—X: Chemical conversion of enmein into enantio-abietane and total synthesis of abientane☆☆☆★

Y. Nagao, E. Fujita, T. Fujita, 1969 .