GC-MS STUDY OF THE IMIDE - AMIDE REARRANGEMENT

DOI: 10.1007/BF00863837

Source and publish data:

Bull. Russ. Acad. Sci. Div. Chem. Sci. (Engl. Transl.) p. 1931 - 1934 (1992)

Update date:2022-08-03

Topics:

Authors:

Gilyarov, V. A.

Shcherbina, T. M.

Laretina, A. P.

Kabachnik, M. I.

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

Article abstract of DOI:10.1007/BF00863837

The imide - amide rearrangement of trialkyl arylimidophosphates by the action of catalytic amounts of boron trifluoride etherate proceeds at least partially by an intermolecular mechanism.Keywords: capillary gas-liquid chromatography/mass spectrometry, im

Full text of DOI:10.1007/BF00863837

Products guided by the article

Product name:trideuteromethyl phenylimidophosphate

Cas No:133827-73-3

R&D Labs maybe for 133827-73-3

SPRING CHEMICAL INDUSTRY CO.,LTD

Contact:86-187-66672125

Address:linchi industry park.zouping
Zhejiang Allied Chemical Co.,Ltd

Contact:18967038207

Address:Area A-30, High-tech Industrial Park, Quzhou, Zhejiang, China.
WENZHOU M&C FOREIGN TRADE CO.,LTD.

Contact:+86-577-88862917

Address:No.8 Liming West Road,Wenzhou,zhejiang,China
Jinan Trio PharmaTech Co., Ltd

Contact:86-531-88811783；+(0)13153010282

Address:2766 Yingxiu Road, Jinan High-Tech Zone, China
Wuhan Better Organic Technology Inc.

Contact:13307163183

Address:Wuhan Economic&Technology Development Zone, Hubei

Relevant to this article

Novel Glycosidation Methodology. The Use of Phenyl Selenoglycosides as Glycosyl Donors and Acceptors in Oligosaccharide Synthesis

Doi:10.1021/jo00064a012
(1993)
Palladium-catalyzed difunctionalization of enol ethers to amino acetals with aminals and alcohols

Doi:10.1021/ja410611b
(2013)
Synthesis, characterization and oscillator-vibrated near-infrared (NIR) luminescence of two pseudo-polymorphic [Yb₄((OH)₂-Salophen)₄] complexes

Doi:10.1016/j.saa.2015.01.082
(2015)
Identification of an elusive catalyst: IrH(η²-C₆H₄P^tBu₂) (Cl) (P^tBu₂Ph) as a precursor for C=C bond migration

Doi:10.1016/s0020-1693(96)05249-8
(1996)
Extensively Conjugated Tetrathiafulvalene (TTF) ?-Electron Donors with Oligothiophenes Spacer Groups

Doi:10.1039/c39930000689
(1993)
Structure-Activity Relationships of β-D-(2S,5R)- and α-D-(2S,5S)-1,3-oxathiolanyl Nucleosides as Potential Anti-HIV Agents

Doi:10.1021/jm00070a006
(1993)

Article Doi