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Dive into the research topics where Takashi Siroi is active.

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Featured researches published by Takashi Siroi.


Tetrahedron Letters | 1981

Chemoselective electrolytic chlorination of methyl group of 3-methyl-3-butenoate moiety of thiazoline-azetidinone homologues

Sigeru Torii; Hideo Tanaka; N. Saitoh; Takashi Siroi; Michio Sasaoka; Junzo Nokami

Abstract Chemoselective electrochlorination of the methyl group on the 3-methyl-3-butenoate moiety of thiazoline-azetidinone derivatives derived from penicillins G and V has been performed in a CH 2 Cl 2 -H 2 O-NaCl-H 2 SO 4 -(Pt or C electrodes) system by adjusting the amount of electricity passed as well as the concentration of Cl − in the media.


Tetrahedron Letters | 1982

Penicillin-cephalosporin conversion III. A Novel route to 3-chloromethyl-Δ3-cephems

Sigeru Torii; Hideo Tanaka; N. Saitoh; Takashi Siroi; Michio Sasaoka; Junzo Nokami

Abstract Synthesis of 3-chloromethyl-Δ 3 -cephems 3 from 4-arenesulfonylthioazetidin-2-ones 1 , derived from penicillins G and V, has been achieved by the electrolytic ene-type chlorination of 1 in a CHC1 3 -aqueous NaCl-H 2 SO 4 -(Pt electrodes) system and subsequent ring closure with NH 3 in DMF.


Tetrahedron Letters | 1982

Penicillin-cephalosporin conversion IV. Direct synthesis of 3'-thiosubstituted cephalosporins from thiazoline-azetidinones

Sigeru Torii; Hideo Tanaka; Michio Sasaoka; N. Saitoh; Takashi Siroi; Junzo Nokami

Direct transformation of thiazoline-azetidinones 2, derived from penicillin G and V, into 3′-thio-substituted cephalosporins 4 has been performed by ring opening of the thiazoline moiety with sulfenyl chlorides followed by ring closure with NH3 in dimethylformamide and simultaneous displacement of the allylic chlorine atom with the leaving thiolates.


Tetrahedron Letters | 1984

Penicillin-cephalosporin conversion X. New synthesis of dithioazetidinones from thiazoline-azetidinones

Sigeru Torii; Hideo Tanaka; Takashi Siroi; Michio Sasaoka

Abstract New ring-opening reaction of thiazoline-azetidinones 1 to dithioazetidinones 2 was achieved with 2-benzothiazolyl disulfide in aqueous acidic media and its potentiality for the preparation of a variety of cephalosporins 3 from various thiazoline-azetidinones 1 is demonstrated.


Tetrahedron Letters | 1984

Penicillin-cephalosporin conversion. XI: Synthesis of 7-(α-substituted phenylacetoamide)cephalosporins by utilization of all the framework elements of penicillin G

Sigeru Torii; Hideo Tanaka; Takashi Siroi; Michio Sasaoka

Abstract A successful synthesis of clinically significant cephalosporins 2a-c with use of all the framework elements of penicillin G is described.


Bulletin of the Chemical Society of Japan | 1983

A convenient synthesis of C(2)-substituted cephalosporins.

Sigeru Torii; Hideo Tanaka; N. Saitoh; Takashi Siroi; Michio Sasaoka; N. Tada; Junzo Nokami


Bulletin of the Chemical Society of Japan | 1983

Penicillin-Cephalosporin Conversion. VII. An Improved Synthesis of 3-Methylenecephams

Shigeru Torii; Hideo Tanaka; Takashi Siroi; Tomoyuki Madono; N. Saitoh; Michio Sasaoka; Junzo Nokami


Bulletin des Sociétés Chimiques Belges | 2010

Prominent Aspects of Electroorganic Synthesis in β‐Lactam Chemistry

Sigeru Torii; Hideo Tanaka; Michio Sasaoka; N. Saitoh; Takashi Siroi; Junzo Nokami


Chemistry Letters | 1981

Electro-hydrogenation of the C=N double bond of thiazoline-azetidinones in an aqueous perchloric acid-dichloromethane-(lead electrodes).

Sigeru Torii; Hideo Tanaka; Makoto Satsuki; Takashi Siroi; N. Saitoh; Michio Sasaoka; Junzo Nokami


Archive | 1989

Azetidinone disulfide derivatives and a process for preparing the same

Sigeru Torii; Hideo Tanaka; Junzo Nokami; Michio Sasaoka; Norio Saito; Takashi Siroi

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Junzo Nokami

Okayama University of Science

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