✦ LIBER ✦

Borontrifluoride Etherate Promoted One-Pot Conversion of Nitriles to Esters

Book ID: 115485538
Publisher: Taylor and Francis Group
Year: 2003
Tongue: English
Weight: 176 KB
Volume: 33
Category: Article
ISSN: 0039-7911
DOI: 10.1081/scc-120024013

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Borontrifluoride Etherate Promoted One-P

Borontrifluoride Etherate Promoted One-Pot Conversion of Nitriles to Esters.

✍ G. Jayachitra; N. Yasmeen; K. Srinivasa Rao; Samuel L. Ralte; R. Srinivasan; A. 📂 Article 📅 2003 🏛 John Wiley and Sons ⚖ 95 KB 👁 2 views

## Abstract For Abstract see ChemInform Abstract in Full Text.

Ultrasound-Promoted “One-Pot” Conversion

Ultrasound-Promoted “One-Pot” Conversion of Nitro Compounds to Carbamates.

✍ S. Chandrasekhar; Ch. Narsihmulu; V. Jagadeshwar 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 28 KB 👁 2 views

Synthesis of triazidochlorosilane (TACS)

Synthesis of triazidochlorosilane (TACS). A novel silicon mediated one pot conversion of aldehydes to nitriles

✍ Saad S. Elmorsy; Abdel-Aziz S. El-Ahl; Hanan Soliman; Fathy A. Amer 📂 Article 📅 1995 🏛 Elsevier Science 🌐 French ⚖ 95 KB

A one-pot conversion of artemisinin to i

A one-pot conversion of artemisinin to its ether derivatives

✍ Chandan Singh; Pallavi Tiwari 📂 Article 📅 2002 🏛 Elsevier Science 🌐 French ⚖ 70 KB

Artemisinin 1 is the active principle of the Chinese traditional antimalarial drug Artemisia annua. 1 Its semi synthetic derivatives, such as artemether 3 and arteether 4 are effective against both chloroquine sensitive and chloroquine resistant P. falciparum and are clinically used for the treatmen

A One-Pot Conversion of Artemisinin to I

A One-Pot Conversion of Artemisinin to Its Ether Derivatives.

✍ Chandan Singh; Pallavi Tiwari 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 26 KB 👁 2 views

A simple one-pot procedure for the conve

A simple one-pot procedure for the conversion of aldehydes to methyl esters

✍ Hakjune Rhee; Jin Yeon Kim 📂 Article 📅 1998 🏛 Elsevier Science 🌐 French ⚖ 260 KB

Ab&ucf: Several methyl esters were obtained by an effkient and simple one-pot procedure from the corresponding aldehydes in high yields. Tbis procedure involves dimethyl acetal formation from aldehydes and subsequent oxidation.