Concepedia

Author

H. ITANI

Shionogi (Japan)

Also Known As

H. ITANI, H. Itani, HIKARU ITANI, Hayam Itani, Hikaru Itani

42

Publications

282

Citations

12

H-Index

29

Concepts

All Affiliations

Shionogi (Japan)Futaba (Japan)
HI

About

H. ITANI is an author at Shionogi (Japan) specializing in organic chemistry, biochemistry, and pharmacology.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Biochemistry

6

6

117

2

Medicine

4

4

72

3

Engineering

3

3

62

4

Natural Sciences

3

3

53

5

Health Sciences

2

2

29

H. ITANI

×

13

Publications

234

Citations

12

H-Index

YearCitations

Bile acids and steroids—XXVII

Ken’ichi Takeda, Taichiro Komeno, Jun’ichi Kawanami,

Tetrahedron

1965

31

A simple and stereocontrolled syntheses of a 1β-methylcarbapenem key intermediate by means of organosilicon chemistry

Shoichiro Uyeo, H. ITANI

Tetrahedron Letters

1991

25

Oxidatively assisted hydrolysis of allylic iodides to rearranged allylic alcohols. A new example of [2,3] sigmatropic rearrangement

Sadao Yamamoto, H. ITANI, Teruji Tsuji,

Journal of the American Chemical Society

1983

24

S-3578, A New Broad Spectrum Parenteral Cephalosporin Exhibiting Potent Activity Against both Methicillin-resistant Staphylococcus aureus (MRSA) and Pseudomonas aeruginosa Synthesis and Structure-activity Relationships.

Hidenori Yoshizawa, H. ITANI, Koji Ishikura,

The Journal of Antibiotics

2002

22

An alternative synthesis of the 1-oxacephem skeleton

Sadao Yamamoto, H. ITANI, Hiroumi Takahashi,

Tetrahedron Letters

1984

21

New broad-spectrum parenteral cephalosporins exhibiting potent activity against both methicillin-resistant Staphylococcus aureus (MRSA) and Pseudomonas aeruginosa. Part 2: Synthesis and structure–activity relationships in the S-3578 series

Hidenori Yoshizawa, Tadatoshi Kubota, H. ITANI,

Bioorganic & Medicinal Chemistry

2004

18

Thiosteroids—XXXIII

Taichiro Komeno, Shoichi Ishihara, H. ITANI

Tetrahedron

1972

17

Solvolyses of 2.alpha.,5-epithio-5.alpha.- and -epoxy-5.alpha.-cholestane derivatives. A reactivity factor of 1011 due to sulfur participation in a 7-thiabicyclo[2.2.1]heptane derivative

Hiroshi Tanida, Teruji Tsuji, Taichiro Komeno,

The Journal of Organic Chemistry

1971

16

New route to 3-(substituted) methyl 1-oxa- and (1-thia)cephems from 3-exomethylene intermediates via sulfenyl chloride adducts

Tsutomu Aoki, Toshiro Konoike, H. ITANI,

Tetrahedron

1983

13

Thiosteroids. XXVI. Steroidal Transannular 2, 5-Epoxide and Related Compounds

Taichiro Komeno, H. ITANI, H. IWAKURA,

Chemical and Pharmaceutical Bulletin

1970

12

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