ACTIVATION OF POLYHALOALKANES BY PALLADIUM CATALYST. PREPARATION OF γ-TRICHLORO KETONES BY THE PALLADIUM CATALYZED ADDITION REACTION OF BROMOTRICHLOROMETHANE AND CARBON TETRACHLORIDE TO ALLYL ALCOHOLS

1981 ◽  
Vol 10 (11) ◽  
pp. 1605-1608 ◽  
Author(s):  
Hideo Nagashima ◽  
Koji Sato ◽  
Jiro Tsuji
Synthesis ◽  
2017 ◽  
Vol 49 (21) ◽  
pp. 4769-4774 ◽  
Author(s):  
Hideki Yorimitsu ◽  
Hayate Saito ◽  
Keisuke Nogi

Borylation of the C–S bond of diaryl sulfoxides with bis(pinacolato)diboron (B2pin2) is accomplished by means of a phosphine-ligated palladium catalyst and LiN(SiMe3)2 as a base. Both of the aryl rings of the diaryl sulfoxides are converted into borylated products.


Molecules ◽  
2022 ◽  
Vol 27 (2) ◽  
pp. 432
Author(s):  
Sulejman Alihodžić ◽  
Hana Čipčić Paljetak ◽  
Ana Čikoš ◽  
Ivaylo Jivkov Elenkov

Unprecedented tandem allylic alkylation/intermolecular Michael addition was used in the preparation of novel bicyclic azalides. NMR spectroscopy was used not only to unambiguously determine and characterize the structures of these unexpected products of chemical reaction but also to investigate the effect the rigid bicyclic modification has on the conformation of the whole molecule. Thus, some of the macrolides prepared showed antibacterial activity in the range of well-known antibiotic drug azithromycin.


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