Oxidative Cyclization Reaction of 2-Aryl-Substituted Cinnamates To Form Phenanthrene Carboxylates by Using MoCl5

2014 ◽  
Vol 20 (39) ◽  
pp. 12463-12469 ◽  
Author(s):  
Kathrin Wehming ◽  
Moritz Schubert ◽  
Gregor Schnakenburg ◽  
Siegfried R. Waldvogel
Synlett ◽  
2018 ◽  
Vol 29 (07) ◽  
pp. 912-917 ◽  
Author(s):  
Parviz Ranjbar ◽  
Narjes Rezaei ◽  
Ehsan Sheikhi

A metal-free oxidative C(sp3)–N coupling process has been developed for the synthesis of 2,3-dihydroquinazolin-4(1H)-ones. The reaction between primary amines, isatoic anhydride, and benzylic alcohols in the presence of HBr in DMSO at 80 °C affords 2,3-dihydroquinazolin-4(1H)-ones in excellent yields. Under these reaction conditions, benzylic alcohols react with in situ generated bromodimethylsulfonium bromide to form alkoxysulfonium intermediates. These intermediates undergo an oxidative cyclization reaction with primary amines and isatoic anhydride to produce the title products.


2012 ◽  
Vol 67 (4) ◽  
pp. 367-372 ◽  
Author(s):  
Jens Preßler ◽  
Rainer Beckert ◽  
Sven Rau ◽  
Roberto Menzel ◽  
Eckhard Birckner ◽  
...  

A synthesis of novel hexacyclic bis-benzimidazoles 6 starting from 2,3-diarylamino-quinoxalines via an oxidative cyclization cascade is described. These very stable and high-melting derivatives are featured by their strong fluorescence in the blue region of the visible spectrum. The cyclization reaction between 2,3-dichloroquinoxaline and 1,2-phenylenediamine did not lead to derivatives of type 6. In this case, only fluoflavine 7 was isolated quantitatively.


2012 ◽  
Vol 90 (3) ◽  
pp. 306-313 ◽  
Author(s):  
Woo-Jin Yoo ◽  
Hao Yuan ◽  
Hiroyuki Miyamura ◽  
Shū Kobayashi

The preparation of 2-substituted benzoxazoles was achieved through a sequential aerobic oxidation – enolization – oxidative cyclization reaction of N-substituted 2-aminophenols catalyzed by platinum nanoclusters supported on a polymer / carbon black composite material.


2014 ◽  
Vol 12 (15) ◽  
pp. 2388-2393 ◽  
Author(s):  
So Won Youn ◽  
Hyoung Sub Song ◽  
Jong Hyub Park

An efficient NHC-catalyzed domino oxidation/oxa-Michael addition reaction of 2-alkenylbenzaldehydes has been developed to afford 3-substituted phthalides bearing a C3-stereogenic center with a broad substrate scope and wide functional group tolerance.


2014 ◽  
Vol 20 (39) ◽  
pp. 12329-12329
Author(s):  
Kathrin Wehming ◽  
Moritz Schubert ◽  
Gregor Schnakenburg ◽  
Siegfried R. Waldvogel

RSC Advances ◽  
2019 ◽  
Vol 9 (41) ◽  
pp. 23876-23887 ◽  
Author(s):  
Thu N. M. Le ◽  
Son H. Doan ◽  
Phuc H. Pham ◽  
Khang H. Trinh ◽  
Tien V. Huynh ◽  
...  

An La0.6Sr0.4CoO3 strontium-doped lanthanum cobaltite perovskite was prepared via a gelation and calcination approach and used as a heterogeneous catalyst for the synthesis of triphenylpyridines via the cyclization reaction between ketoximes and phenylacetic acids.


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