Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Ebenezer Ametsetor"'
Publikováno v:
Molecules, Vol 29, Iss 14, p 3406 (2024)
A one-pot [3+3] aldol-SNAr-dehydration annulation sequence was utilized to fuse hindered phenols onto aromatic substrates. The transformation joins doubly activated 1,3-disubstituted acetone derivatives (dinucleophiles) with C5-activated 2-fluorobenz
Externí odkaz:
https://doaj.org/article/9588f2d2a91c486982656f405c87858f
Publikováno v:
Molecules, Vol 28, Iss 15, p 5856 (2023)
A domino aldol-SNAr-dehydration [3+3] annulation strategy has been utilized to fuse six-membered cyclic amides onto aromatic substrates. 2-Arylacetamides have been reacted with 2-fluorobenzaldehyde derivatives activated toward SNAr reaction by an ele
Externí odkaz:
https://doaj.org/article/770ba6d49ce54e82a4e4d16a8849e1bd
Publikováno v:
Molecules, Vol 28, Iss 7, p 3256 (2023)
A series of new Morita–Baylis–Hillman acetates were prepared and reacted with methanesulfonamide (K2CO3, DMF, 23 °C) to produce tertiary dihydroquinoline sulfonamides in high yields. Subsequent efforts to eliminate the methylsulfonyl group from
Externí odkaz:
https://doaj.org/article/7ab055f8f79b4fccab04845c1b5fb870
Publikováno v:
Molecules, Vol 27, Iss 20, p 6998 (2022)
A new synthesis of C5-substituted 1-alkyl-1H-indole-3-carboxylic esters is reported. A series of methyl 2-arylacrylate aza-Michael acceptors were prepared with aromatic substitution to activate them towards SNAr reaction. Subsequent reaction with a s
Externí odkaz:
https://doaj.org/article/99cbc276fd4b42409f306ee48c031ec0
Publikováno v:
Molecules, Vol 26, Iss 4, p 890 (2021)
An efficient synthetic route to highly substituted dihydroquinolines and dihydronaphthyridines has been developed using a domino reaction of Morita-Baylis-Hillman (MBH) acetates with primary aliphatic and aromatic amines in DMF at 50–90 °C. The MB
Externí odkaz:
https://doaj.org/article/709ff66734a24349acad2239861e379c
Publikováno v:
Molecules, Vol 25, Iss 21, p 5168 (2020)
An efficient synthetic route to highly functionalized naphthalenes and quinolines has been developed using domino reactions between Morita–Baylis–Hillman (MBH) acetates and active methylene compounds (AMCs) promoted by anhydrous K2CO3 in dry N,N-
Externí odkaz:
https://doaj.org/article/0651300fc8904819ab19dd16338ecd07
Publikováno v:
Molecules
Molecules, Vol 25, Iss 5168, p 5168 (2020)
Volume 25
Issue 21
Molecules, Vol 25, Iss 5168, p 5168 (2020)
Volume 25
Issue 21
An efficient synthetic route to highly functionalized naphthalenes and quinolines has been developed using domino reactions between Morita&ndash
Baylis&ndash
Hillman (MBH) acetates and active methylene compounds (AMCs) promoted by anhydrous
Baylis&ndash
Hillman (MBH) acetates and active methylene compounds (AMCs) promoted by anhydrous