Reactivity in the Gas Phase. Behaviour of Isoxazoles under Negative Ion Chemical Ionization Conditions

DOI: 10.1002/oms.1210240709

Source and publish data:

Organic Mass Spectrometry p. 490 - 496 (1989)

Update date:2022-08-05

Topics:

Authors:

Guarna, Antonio

Moneti, Gloriano

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

Article abstract of DOI:10.1002/oms.1210240709

+>^- ions of isoxazole (1a), 3-methylisoxazole (1b), 5-methylisoxazole (1c), 5-phenylisoxazole (1d) and benzoylacetonitrile (2a) are generated using NICI/OH^- or NICI/NH2^- techniques.Their fragmentation pathwa

Full text of DOI:10.1002/oms.1210240709

Products guided by the article

Product name:4-<2H>-5-phenylisoxazole

Cas No:125344-13-0

R&D Labs maybe for 125344-13-0

shanghai payne pharm co.,ltd.

Contact:+86-021-58123769

Address:No.780 of Cailun Road,Zhangjiang Hi-tech Park,Pudong,Shanghai
LINYI FUDE FINE CHEMICAL CO.,LTD

Contact:86-539-2361184

Address:YISHUI, LINYI,SAHNDONG,CHINA
Laizhou City Laiyu Chemical CO.,Ltd

Contact:+86-535-2719337/2719339

Address:Chenggang road zhuyou laizhou City Shangdong China
Changsha Yonta Industry Co., Ltd.

Contact:+ 86-731-8535 2228

Address:Rm.1717, North Bldg., No.368, East 2nd Ring Road(2nd Section)
Lian Xing Chemical Co.,Ltd.

Contact:0792-8228321

Address:10TH Floor No.121 binjiang Road Xunyang District

Relevant to this article

Design of a series of bicyclic HIV-1 integrase inhibitors. Part 1: Selection of the scaffold

Doi:10.1016/j.bmcl.2010.07.079
(2010)
Copper-mediated oxidative cyclization of heterocyclically substituted aldimines

Doi:10.3987/COM-10-11966
(2010)
Enynones in Organic Synthesis. 8. Synthesis of the Antimicrobial-Cytotoxic Agent Juncusol and Members of the Effusol Class of Phenols

Doi:10.1021/jo00107a017
(1995)
High nonlinear optical response in 4-chlorothiazole-based azo dyes

Doi:10.1016/j.dyepig.2010.07.011
(2011)
Thiophene-fused phospholo[3,2-b]phospholes and their dichalcogenides: Synthesis and structure-photophysical properties relationships

Doi:10.1016/j.crci.2010.04.021
(2010)
Doi:10.1021/ja01606a007
(1955)

Article Doi