Enol ether formation by disproportionation of the 1,5-biradical intermediate in the photocyclization of o-isopropoxybenzophenone

DOI: 10.1016/S0040-4039(00)92114-2

Source and publish data:

Tetrahedron Letters p. 895 - 898 (1991)

Update date:2022-09-26

Topics:

Authors:

Wagner Wagner

Laidig Laidig

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

Article abstract of DOI:10.1016/S0040-4039(00)92114-2

The 1,3-dioxane formed by uv irradiation of o-isopropoxybenzophenone is produced by intramolecular cyclization of a hydroxy enol ether, the disproportionation product of the 1,5-biradical formed by triplet state hydrogen abstraction. The enol ether is stable in the absence of acid.

Full text of DOI:10.1016/S0040-4039(00)92114-2

Products guided by the article

Product name:2,2-Dimethyl-4-phenyl-4H-benzo[1,3]dioxine

Cas No:133745-31-0

R&D Labs maybe for 133745-31-0

Changzhou naidechemical Co.Ltd

Contact:+86-519-82589807

Address:NO.25,Houyang street,Jintan,Changzhou City
Xi'an Unique Electronic and Chemical Co., Ltd.

Contact:+86-029-88238008

Address:1703# B BUILDING WEST ELECTRONIC ZONE, XI'AN, CHINA
Lian Xing Chemical Co.,Ltd.

Contact:0792-8228321

Address:10TH Floor No.121 binjiang Road Xunyang District
Jiangsu Willing Bio-Tech Co ltd

website:http://www.willingbio.com/

Contact:+86 18796908173

Address:No 18 Guoqiao Road
XI'AN CHUKANG BIOTECHNOLOGY CO.,LTD

Contact:29-63685658 63685359

Address:Room 3-1202,Building 1,Oriental oasis,East of Xianning Road,Xi'an,Shaanxi 710043 P.R.China

Relevant to this article

Macrocyclization of Peptide Side Chains by the Ugi Reaction: Achieving Peptide Folding and Exocyclic N-Functionalization in One Shot

Doi:10.1021/acs.joc.5b00858
(2015)
Synthesis and biological evaluation of 1,2,3-triazole linked aminocombretastatin conjugates as mitochondrial mediated apoptosis inducers

Doi:10.1016/j.bmc.2014.08.008
(2014)
Bis(cyclopentadienyldicarbonyliron) as a convenient carbon monoxide source in palladium-catalyzed carbonylative coupling of aryl iodides with amines, alcohols, and thiols

Doi:10.1246/cl.2011.904
(2011)
Ca(OH)₂-mediated efficient synthesis of 2-amino-5-hydroxy-4H- chromene derivatives with various substituents

Doi:10.1016/j.tet.2011.08.086
(2011)
Thiophene as a structural element of physiologically active compounds. 19. The synthesis of substituted (6H-thieno[2,3-b]pyrrol-4-yl)phenylmethanones

Doi:10.1002/ardp.19913240406
(1991)
Iridium complex-catalyzed allylic alkylation of allylic esters and allylic alcohols: Unique regio- and stereoselectivity

Doi:10.1021/ja981560p
(1998)

Article Doi