Rearrangement Reactions of Tritylcarbenes: Surprising Ring Expansion and Computational Investigation

E-ISSN： 1521-3765|21|42|14911-14923

ISSN： 0947-6539

Source： CHEMISTRY - A EUROPEAN JOURNAL, Vol.21, Iss.42, 2015-10, pp. : 14911-14923

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

Synthesis of Macrocyclic Ketones by Repeatable Two-Carbon Ring Expansion Reactions

By Nagel Matthias Fráter Georg Hansen Hans-Jürgen

CHIMIA International Journal for Chemistry, Vol. 57, Iss. 4, 2003-04 ,pp. : 196-199

Swiss Chemical Society

Access to resources Recommend Favorite

Visible‐Light Photoredox‐Catalyzed Semipinacol‐Type Rearrangement: Trifluoromethylation/Ring Expansion by a Radical–Polar Mechanism

ANGEWANDTE CHEMIE INTERNATIONAL EDITION, Vol. 54, Iss. 39, 2015-09 ,pp. : 11577-11580

John Wiley & Sons Inc

Access to resources Recommend Favorite

Ring contraction in reactions of 3-benzoylquinoxalin-2-ones with 1,2-phenylenediamines. Quinoxaline-benzoimidazole rearrangement

By Mamedov V. A. Kalinin A. A. Gubaidullin A. T. Chernova A. V. Litvinov I. A. Levin Ya. A. Shagidullin R. R.

Russian Chemical Bulletin, Vol. 53, Iss. 1, 2004-01 ,pp. : 164-175

Springer Publishing Company

Access to resources Recommend Favorite

Diaziridine ring expansion in 6-aryl-1,5-diazabicyclo[3.1.0]hexanes upon reactions with activated olefins in ionic liquids

By Syroeshkina Yu. Fershtat L. Kachala V. Kuznetsov V. Makhova N.

Russian Chemical Bulletin, Vol. 59, Iss. 8, 2010-08 ,pp. : 1621-1630

Springer Publishing Company

Access to resources Recommend Favorite

Synthesis of Carbazole Alkaloids by Ring‐Closing Metathesis and Ring Rearrangement–Aromatization

ANGEWANDTE CHEMIE, Vol. 127, Iss. 52, 2015-12 ,pp. : 16057-16061

John Wiley & Sons Inc

Access to resources Recommend Favorite