Pyridonecarboxylic acids as antibacterial agents. V. Synthesis of 1-vinyl-1,4-dihydro-4-oxo-1,8- and 1,6-naphthyridine-3-carboxylic acids

DOI: 10.1248/cpb.33.4402

Source and publish data:

Chemical and Pharmaceutical Bulletin p. 4402 - 4408 (1985)

Update date:2022-08-03

Topics:

Authors:

Mishio Mishio

Hirose Hirose

Minamida

Matsumoto

Read Full Text PDF DownLoad Join now for total 90,000,000 free articles

Article abstract of DOI:10.1248/cpb.33.4402

Full text of DOI:10.1248/cpb.33.4402

NII-Electronic Library Service

Products guided by the article

Product name:7-(4-Benzyl-piperazin-1-yl)-1-(2-chloro-ethyl)-4-oxo-1,4-dihydro-[1,6]naphthyridine-3-carboxylic acid ethyl ester

Cas No:58368-81-3

R&D Labs maybe for 58368-81-3

Nanjing distinctions Medical Technology Co., Ltd.(expird)

Contact:+86-15996203785 13914714059

Address:nanjing,jiangsu , China
Shandong Shouguang Songchuan Industrial Additives Co.,Ltd

Contact:+86-536-8566856

Address:Shouguang,Shandong,China
JIANGXI XINXIN CHEMICAL CO., LTD.

Contact:86-15957176628

Address:INDUSTRY ROAD 1, INDUSTRIAL PARK, HEKOU TOWN,YANSHAN COUNTY, JIANGXI PROVINCE, CHINA
Shanghai Yurui Biotechnology(Anyang) Pharmaceutical Co., Ltd

Contact:+86-0372-3662335 +86-0372-3661988

Address:hanling industrial park anyang
Radiant Pharma & Tech Company

Contact:+86-511-88790000

Address:338 North Yushan Rd, Zhenjiang, Jiangsu 212016

Relevant to this article

Doi:10.1021/ja00418a042
(1976)
Nonpeptide α_vβ₃ Antagonists. 8. In Vitro and in Vivo Evaluation of a Potent α_vβ₃ Antagonist for the Prevention and Treatment of Osteoporosis

Doi:10.1021/jm030306r
(2003)
L-proline catalyzed unprecedented synthesis of novel naphtho-bis[1,3]oxazines under solvent-free conditions

Doi:10.1080/00397911.2020.1719423
(2020)
Doi:10.1016/S0040-4039(00)91182-1
(1975)
Total synthesis of (±)-kainic acid: A photochemical C-H carbamoylation approach

Doi:10.1021/ol200772f
(2011)
Supported dual-acidic 1,3-disulfoimidazolium chlorozincate@HZSM-5 as a promising heterogeneous catalyst for synthesis of indole derivatives

Doi:10.1002/aoc.4672
(2019)

Article Doi