𝔖 Bobbio Scriptorium
✦   LIBER   ✦

1-(Cyanomethyl)benzotriazole as a Convenient Precursor for the Synthesis of 2-Substituted Thiazoles

✍ Scribed by Katritzky, Alan R.; Chen, Jie; Yang, Zhijun

Book ID
120543031
Publisher
American Chemical Society
Year
1995
Tongue
English
Weight
634 KB
Volume
60
Category
Article
ISSN
0022-3263

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

2-Trifluoroacetyl-1-methoxycycloalkenes:
2-Trifluoroacetyl-1-methoxycycloalkenes: A convenient precursor for the synthesis of geminated polymethylene trifluoromethyl substituted heterocycles
✍ Helio Gauze Bonacorso; Michelle Budke Costa; Cleber AndrΓ© Cechinel; Ronan Carlo πŸ“‚ Article πŸ“… 2009 πŸ› Journal of Heterocyclic Chemistry 🌐 English βš– 105 KB πŸ‘ 1 views

## Abstract magnified image This article describes the methodology that allows the simultaneous introduction of a trifluoromethyl group and a 7‐, 8‐, and 10‐membered cycloalkane ring fused to heterocyclic derivatives. A series of 10 geminated polymethylene trifluoromethyl substituted isoxazolines,

A convenient synthesis of 8-substituted
A convenient synthesis of 8-substituted indolizines as precursors to 5-substituted cycl{3.2.2}azine derivatives
✍ Jonathan O. Smith; Braja K. Mandal πŸ“‚ Article πŸ“… 1997 πŸ› Journal of Heterocyclic Chemistry 🌐 English βš– 462 KB

## Abstract The synthesis of 8‐substituted indolizines is described __via__ a two step process in which a 1,4‐diketone, containing a rerf‐butyl group, is cyclocondensed with a trialkylsilyl protected pyrrole to provide 5,8‐disubstituted indolizines in higher yields than the identical reaction with

ChemInform Abstract: A Convenient Synthe
ChemInform Abstract: A Convenient Synthesis of 8-Substituted Indolizines as Precursors to 5-Substituted Cycl{3.2.2}azine Derivatives.
✍ J. O. SMITH; B. K. MANDAL πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 33 KB πŸ‘ 2 views

A Convenient Synthesis of 8-Substituted Indolizines as Precursors to 5-Substituted Cycl{3.2.2}azine Derivatives. -A simple and efficient approach for the title precursors (V), which are useful for the synthesis of the azine derivatives (VII), is presented. It is noteworthy that the first step also