ChemInform Abstract: THERMOLYSIS OF TERTIARY ALKYL AZIDES

1974 ◽  
Vol 5 (14) ◽  
pp. no-no
Author(s):  
R. A. ABRAMOVITCH ◽  
E. P. KYBA
Keyword(s):  
Alkyl Azides ◽  
Tertiary Alkyl

scholarly journals Sulfonium Ion-Promoted Traceless Schmidt Reaction of Alkyl Azides

2021 ◽  
Author(s):  
Bayu Ardiansah ◽  
Hiroki Tanimoto ◽  
Takenori Tomohiro ◽  
Tsumoru Morimoto ◽  
Kiyomi Kakiuchi
Keyword(s):  
Ring Opening ◽  
One Pot ◽  
Schmidt Reaction ◽  
Alkyl Azides ◽  
Sulfonium Ions ◽  
Bond Scission ◽  
Imine Compounds ◽  
Tertiary Alkyl

Schmidt reaction by sulfonium ions is described. General primary, secondary, and tertiary alkyl azides were converted to the corresponding carbonyl or imine compounds without any trace of the activators. This bond scission reaction showcased ring-opening, -expansion, and one-pot further conversion of the substrates as well as the application with C-H azidation.

scholarly journals Sulfonium Ion-Promoted Traceless Schmidt Reaction of Alkyl Azides

2021 ◽  
Author(s):  
Bayu Ardiansah ◽  
Hiroki Tanimoto ◽  
Takenori Tomohiro ◽  
Tsumoru Morimoto ◽  
Kiyomi Kakiuchi
Keyword(s):  
Ring Opening ◽  
One Pot ◽  
Schmidt Reaction ◽  
Alkyl Azides ◽  
Sulfonium Ions ◽  
Bond Scission ◽  
Imine Compounds ◽  
Tertiary Alkyl

Schmidt reaction by sulfonium ions is described. General primary, secondary, and tertiary alkyl azides were converted to the corresponding carbonyl or imine compounds without any trace of the activators. This bond scission reaction showcased ring-opening, -expansion, and one-pot further conversion of the substrates as well as the application with C-H azidation.

Preparation of Tertiary Alkyl Azides

1971 ◽  
Vol 10 (6) ◽  
pp. 412-413 ◽  
Author(s):  
Paul Margaretha ◽  
Sonja Solar ◽  
Oskar E. Polansky
Keyword(s):  
Alkyl Azides ◽  
Tertiary Alkyl

scholarly journals Sulfonium Ion-Promoted Traceless Schmidt Reaction of Alkyl Azides

2021 ◽  
Author(s):  
Bayu Ardiansah ◽  
Hiroki Tanimoto ◽  
Takenori Tomohiro ◽  
Tsumoru Morimoto ◽  
Kiyomi Kakiuchi
Keyword(s):  
Ring Opening ◽  
One Pot ◽  
Schmidt Reaction ◽  
Alkyl Azides ◽  
Sulfonium Ions ◽  
Bond Scission ◽  
Imine Compounds ◽  
Tertiary Alkyl

Schmidt reaction by sulfonium ions is described. General primary, secondary, and tertiary alkyl azides were converted to the corresponding carbonyl or imine compounds without any trace of the activators. This bond scission reaction showcased ring-opening, -expansion, and one-pot further conversion of the substrates as well as the application with C-H azidation.

Thermolysis of tertiary alkyl azides

1974 ◽  
Vol 96 (2) ◽  
pp. 480-488 ◽  
Author(s):  
R. A. Abramovitch ◽  
E. P. Kyba
Keyword(s):  
Alkyl Azides ◽  
Tertiary Alkyl

Migration aptitudes in the photolysis of some tertiary alkyl azides

1976 ◽  
Vol 41 (14) ◽  
pp. 2368-2372 ◽  
Author(s):  
Frederick C. Montgomery ◽  
William H. Saunders
Keyword(s):  
Alkyl Azides ◽  
Tertiary Alkyl

Synthesis of tertiary alkyl azides

1975 ◽  
Vol 16 (34) ◽  
pp. 2959-2960 ◽  
Author(s):  
J.A. Miller
Keyword(s):  
Alkyl Azides ◽  
Tertiary Alkyl

Sulfonium Ion-Promoted Traceless Schmidt Reaction of Alkyl Azides

2021 ◽  
Author(s):  
Bayu Ardiansah ◽  
Hiroki Tanimoto ◽  
Takenori Tomohiro ◽  
Tsumoru Morimoto ◽  
Kiyomi Kakiuchi
Keyword(s):  
Schmidt Reaction ◽  
Alkyl Azides ◽  
Sulfonium Ions ◽  
Imine Compounds ◽  
Tertiary Alkyl

Schmidt reaction by sulfonium ions is described. General primary, secondary, and tertiary alkyl azides were converted to the corresponding carbonyl or imine compounds without any trace of the activators. This...

Sign in / Sign up

Export Citation Format

Share Document