ChemInform Abstract: Convenient Synthesis of Heteroaryl-Linked Benzimidazoles via Microwave-Assisted Boronate Ester Formation.

ChemInform ◽  
2009 ◽  
Vol 40 (29) ◽  
Author(s):  
Tara R. Rheault ◽  
Kelly H. Donaldson ◽  
Mui Cheung
Keyword(s):  
Boronate Ester ◽  
Microwave Assisted ◽  
Convenient Synthesis ◽  
Ester Formation

Microwave-Assisted Convenient Synthesis ofα,β-Unsaturated Esters and KetonesviaAldol-Adduct Elimination

2013 ◽  
Vol 96 (8) ◽  
pp. 1548-1559 ◽  
Author(s):  
Pathi Suman ◽  
Rayala Nageswara Rao ◽  
Bhimapaka China Raju
Keyword(s):  
Unsaturated Esters ◽  
Microwave Assisted ◽  
Convenient Synthesis

Microwave-Assisted Facile and Convenient Synthesis of Imidazolines.

ChemInform ◽  
2004 ◽  
Vol 35 (8) ◽  
Author(s):  
I. Mohammadpoor-Baltork ◽  
M. Abdollahi-Alibeik
Keyword(s):  
Microwave Assisted ◽  
Convenient Synthesis

scholarly journals On the rate of boronate ester formation inortho-aminomethyl-functionalised phenyl boronic acids

2013 ◽  
Vol 25 (2) ◽  
pp. 79-86 ◽  
Author(s):  
Byron E. Collins ◽  
Pedro Metola ◽  
Eric V. Anslyn
Keyword(s):  
Boronic Acids ◽  
Boronate Ester ◽  
Ester Formation

ChemInform Abstract: Microwave-Assisted Ester Formation Using O-Alkylisoureas: A Convenient Method for the Synthesis of Esters with Inversion of Configuration.

ChemInform ◽  
2009 ◽  
Vol 40 (49) ◽  
Author(s):  
Alessandra Chighine ◽  
Stefano Crosignani ◽  
Marie-Claire Arnal ◽  
Mark Bradley ◽  
Bruno Linclau
Keyword(s):  
Convenient Method ◽  
Microwave Assisted ◽  
Ester Formation

scholarly journals A Convenient Synthesis of (16S,20S)-3β-Hydroxy-5α-pregnane-20,16-carbolactam and Its N-alkyl Derivatives

Molecules ◽  
2020 ◽  
Vol 25 (10) ◽  
pp. 2377
Author(s):  
Agnieszka Wojtkielewicz ◽  
Damian Pawelski ◽  
Przemysław Bazydło ◽  
Aneta Baj ◽  
Stanisław Witkowski ◽  
...  
Keyword(s):  
Ring Opening ◽  
Reductive Amination ◽  
Lactone Ring ◽  
Synthetic Route ◽  
Microwave Assisted ◽  
Alkyl Derivatives ◽  
Convenient Synthesis

A concise synthesis of (16S,20S)-3β-hydroxy-5α-pregnane-20,16-carbolactam from tigogenin via the corresponding lactone is described. The most efficient synthetic route consisted of the lactone ring-opening with aminoalane reagent followed by PDC or Dess-Martin oxidation. The oxo-amide obtained was subjected to cyclization with Et3SiH/TFA or Et3SiH/Bi(TfO)3. Alternately, the lactone was converted first to the oxo-acid, which was then subjected to the microwave-assisted reductive amination. N-Alkyl derivatives were also obtained in a similar way.

Microwave assisted convenient synthesis of quino[2,3-b][1,5]benzoxazepines

2009 ◽  
Vol 20 (5) ◽  
pp. 557-561 ◽  
Author(s):  
Swapnil S. Sonar ◽  
Sandip A. Sadaphal ◽  
Shivaji S. Pawar ◽  
Bapurao B. Shingate ◽  
Murlidhar S. Shingare
Keyword(s):  
Microwave Assisted ◽  
Convenient Synthesis

Microwave-Assisted Beckmann Rearrangement: Convenient Synthesis of 1,3-Diaza-bicyclo[3.2.2]nonane.

ChemInform ◽  
2006 ◽  
Vol 37 (23) ◽  
Author(s):  
Michael P. Curtis ◽  
William H. Bunnelle ◽  
Thomas G. Pagano ◽  
Murali Gopalakrishnan ◽  
Ramin Faghih
Keyword(s):  
Beckmann Rearrangement ◽  
Microwave Assisted ◽  
Convenient Synthesis
Sign in / Sign up

Export Citation Format

Share Document