𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Synthesis of Tertiary Amides from Anionically Activated Aromatic Trifluoromethyl Groups

✍ Scribed by O’Mahony, Gavin; Pitts, Andrew K.

Book ID
111656879
Publisher
American Chemical Society
Year
2010
Tongue
English
Weight
253 KB
Volume
12
Category
Article
ISSN
1523-7060

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: Unexpected C—C Bond
ChemInform Abstract: Unexpected C—C Bond Cleavage: Synthesis of 1,2,4-Oxadiazol-5-ones from Amidoximes with Pentafluorophenyl or Trifluoromethyl Anion Acting as Leaving Group.
✍ Thibaud Gerfaud; Hai-Long Wei; Luc Neuville; Jieping Zhu 📂 Article 📅 2012 🏛 John Wiley and Sons ⚖ 32 KB 👁 1 views

## Abstract A novel method for the synthesis of 1,2,4‐oxadiazol‐5‐ones (III) and (VI) is elaborated using an acylation reaction of amidoximes (I) and (IV) with TFAA or pentafluorobenzoyl chloride followed by a spontaneous C—C bond breaking with the release of fluoroform or pentafluorobenzene, respe

Application of microwave irradiation for
Application of microwave irradiation for synthesis of novel optically active poly(amide imides) derived from diacid chloride containing epiclon and L-isoleucine with aromatic diamines
✍ Shadpor Mallakpour; Elaheh Kowsari 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 English ⚖ 299 KB 👁 2 views

## Abstract Epiclon [3a,4,5,7a‐tetrahydro‐7‐methyl‐5‐(tetrahydro‐2,5‐dioxo‐3‐furanyl)‐1,3‐isobenzofurandione] or [5‐(2,5‐dioxotetrahydrofurfuryl)‐3‐methyl‐3‐cyclohexyl‐1,2‐dicarboxylic acid anhydride] (1) was reacted with L‐isoleucine (2) in acetic acid and the resulting imide acid (3) was obtained