Sean "PDF" Bride Career DIENONE PHENOL REARRANGEMENT PDF

DIENONE PHENOL REARRANGEMENT PDF

Re2O7 Catalyzed Dienone-Phenol Rearrangement. Zilei Xia,a,b,ǁ Jiadong Hu,a, b,ǁ Zhigao Shen,a,b Qizheng Yao*,a and Weiqing Xie*,b,c a Department of. Dienone–phenol rearrangement of 8,8-dimethyl- and 6,8,8-trimethyl-naphthalene -1,4,5(8H)-triones (1) and (2) in acetic anhydride as solvent is the subject of a. The experiment is based on the dienone-phenol rearrangement reaction of the sesquiterpene santonin to give -desmotroposantonin acetate. It challenges.

Author: Vitilar Meztijinn
Country: China
Language: English (Spanish)
Genre: Life
Published (Last): 10 January 2014
Pages: 181
PDF File Size: 1.97 Mb
ePub File Size: 13.16 Mb
ISBN: 228-2-86990-749-5
Downloads: 94813
Price: Free* [*Free Regsitration Required]
Uploader: Vudolrajas

Chemical Forums

Jump to main content. Journal of the Chemical Society, Perkin Transactions 2. Jump to site search. Fetching data from CrossRef.

The effect of temperature in the reaction of 1 and that of the C-6 phnol group of 2 are discussed. You do not have JavaScript enabled.

The effects of sulphuric and acetic acids are also investigated. XX is the XXth reference in the list of references.

Please enable JavaScript to access the full features of the site or access our non-JavaScript page. If you are not the author of this article and you wish to reproduce material from it in a third party non-RSC publication you must formally request permission using Copyright Clearance Center.

Dienone—phenol rearrangement dienoone of 8,8-dimethyl- and 6,8,8-trimethyl-naphthalene-1,4,5 8 H -triones in acetic anhydride solution.

Back to tab navigation Fetching data from CrossRef. Previous Article Next Article. Both substrates show limiting [H 2 SO 4 ] dependence and an inhibiting effect with acetic acid.

There was a problem providing the content you requested

In all cases the Ref. For reproduction of material from NJC: Dienone—phenol rearrangemejt mechanism of 8,8-dimethyl- and 6,8,8-trimethyl-naphthalene-1,4,5 8 H -triones in acetic anhydride solution C. Reproduced material should be attributed as follows: If the material has been adapted instead of reproduced from the original RSC publication “Reproduced from” can be substituted with “Adapted from”.

Back to tab navigation. For reproduction of material from PCCP: If you are the author of this article you do not need to formally request permission to reproduce figures, diagrams etc.

If you are the author of this article you still need to obtain permission to reproduce the whole article in a third party publication with the exception of reproduction of the whole article in a thesis or dissertation.

For reproduction of material from PPS: The results are rationalized in terms of the formation of acylated intermediate cations and schematic representation is provided. This may take some time to load. Go to our Instructions for using Copyright Clearance Center page for details.

Dienone-phenol rearrangement

Dienone—phenol rearrangement of 8,8-dimethyl- and 6,8,8-trimethyl-naphthalene-1,4,5 8 H -triones 1 and 2 in acetic anhydride as solvent is the subject of a kinetic study.

Information about reproducing material from RSC articles with different licences is available on our Permission Requests page. Authors contributing to RSC publications journal articles, books or book chapters do not need to formally request permission to reproduce material contained in this article provided that the correct acknowledgement is given with the reproduced material.

For reproduction of material from all other RSC journals and books: Search articles by author Candelaria Goycoolea. Back to tab navigation Download options Please wait