ROLE OF ELECTROSYNTHETIC METHODOLOGY ON FUNCTIONALIZATION OF beta -LACTAMS

Sigeru Torri; Hideo Tanaka

ROLE OF ELECTROSYNTHETIC METHODOLOGY ON FUNCTIONALIZATION OF beta -LACTAMS

Sigeru Torri
, Hideo Tanaka

研究成果 › 査読

抄録

Chemical conversion of penicillin into cephalosporin has been a subject of intensive studies. The problems laid on elaborating synthesis of cephalosporin are as follows: (1) construction of cephem nuclea, (2) introduction of C(3) pendants, and (3) modification of C(7) amide pendants. We found that electrolytic ene-type chlorination of thiazolineazetidinones derived from penicillins is an efficient procedure to prove problem (2) and to solve problem (3).

本文言語	English
ページ（範囲）	465
ページ数	1
ジャーナル	Electrochemical Society Extended Abstracts
巻	84-1
出版ステータス	Published - 1984
外部発表	はい

ASJC Scopus subject areas

工学一般

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title = "ROLE OF ELECTROSYNTHETIC METHODOLOGY ON FUNCTIONALIZATION OF beta -LACTAMS",

abstract = "Chemical conversion of penicillin into cephalosporin has been a subject of intensive studies. The problems laid on elaborating synthesis of cephalosporin are as follows: (1) construction of cephem nuclea, (2) introduction of C(3) pendants, and (3) modification of C(7) amide pendants. We found that electrolytic ene-type chlorination of thiazolineazetidinones derived from penicillins is an efficient procedure to prove problem (2) and to solve problem (3).",

author = "Sigeru Torri and Hideo Tanaka",

year = "1984",

language = "English",

volume = "84-1",

pages = "465",

journal = "Electrochemical Society Extended Abstracts",

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TY - JOUR

T1 - ROLE OF ELECTROSYNTHETIC METHODOLOGY ON FUNCTIONALIZATION OF beta -LACTAMS

AU - Torri, Sigeru

AU - Tanaka, Hideo

PY - 1984

Y1 - 1984

N2 - Chemical conversion of penicillin into cephalosporin has been a subject of intensive studies. The problems laid on elaborating synthesis of cephalosporin are as follows: (1) construction of cephem nuclea, (2) introduction of C(3) pendants, and (3) modification of C(7) amide pendants. We found that electrolytic ene-type chlorination of thiazolineazetidinones derived from penicillins is an efficient procedure to prove problem (2) and to solve problem (3).

AB - Chemical conversion of penicillin into cephalosporin has been a subject of intensive studies. The problems laid on elaborating synthesis of cephalosporin are as follows: (1) construction of cephem nuclea, (2) introduction of C(3) pendants, and (3) modification of C(7) amide pendants. We found that electrolytic ene-type chlorination of thiazolineazetidinones derived from penicillins is an efficient procedure to prove problem (2) and to solve problem (3).

UR - https://www.scopus.com/pages/publications/17344381898

UR - https://www.scopus.com/pages/publications/17344381898#tab=citedBy

M3 - Conference article

AN - SCOPUS:17344381898

SN - 0160-4619

VL - 84-1

SP - 465

JO - Electrochemical Society Extended Abstracts

JF - Electrochemical Society Extended Abstracts

ER -

ROLE OF ELECTROSYNTHETIC METHODOLOGY ON FUNCTIONALIZATION OF beta -LACTAMS

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