Results 301 to 310 of about 64,220 (327)

Radical Aminomethylation of Imines

The Journal of Organic Chemistry, 2014
Taking advantage of the high level of performance of N-alkoxycarbonyl-imines, we achieved the first example of addition of the aminomethyl radical to imine. The reaction efficiency depended on the structure of the radical precursor, whether it is an iodide or a xanthate, and an electron-withdrawing group on the nitrogen atom of the radical.
Shintaro, Fujii, Takehito, Konishi, Yusuke, Matsumoto, Yousuke, Yamaoka, Kiyosei, Takasu, Ken-Ichi, Yamada   +5 more
openaire   +2 more sources

1.3-additionen mit pyridin-imin, chinolin-imin, isochinolin-imin und phenanthridin-imin

Tetrahedron Letters, 1962
Rolf Huisgen, Rudolf Grashey, Roland Krischke   +2 more
openaire   +1 more source

Acraldehyde Imine and 2‐Methylacraldehyde Imine

Angewandte Chemie International Edition in English, 1967
B. Bogdanović, M. Velić
openaire   +1 more source

Aziridine Imines

Angewandte Chemie International Edition in English, 1970
Helmut Quast, Edeltraud Schmitt
openaire   +1 more source

IMINES

1986
Stanley R. Sandler, Wolf Karo
openaire   +1 more source

Synthesis from Imines and Imine Derivatives

2012
F. Chemla, F. Ferreira, A. Pérez-Luna
openaire   +1 more source

imine, n.

2023
openaire   +1 more source

Imine Alkylation

2008
C. J. Forsyth, T. J. Murray
openaire   +1 more source

Imines

1971
openaire   +1 more source

With Imines

2006
C. Palomo, M. Oiarbide, J. M. Aizpurua
openaire   +2 more sources