quinolines in a sentence
SentencesMobile
- The Perkow reaction is also used in the synthesis of novel quinolines.
- Much of the asymmetric hydrogenation chemistry of quinoxalines is closely related to that of the structurally similar quinolines.
- With much of the literature on the synthesis of quinolines, there is some discrepancy on whether keto form ) predominates.
- Methods designed specifically for 2-substituted pyridine hydrogenation can involve asymmetric systems developed for related substrates like 2-substituted quinolines and quinoxalines.
- Some common examples of secondary metabolites include : ergot alkaloids, antibiotics, naphthalenes, nucleosides, phenazines, quinolines, terpenoids, peptides and growth factors.
- Such hydroxy-substituted quinolines are, most often, not distinguished from a particular isomeric form termed a tautomer ( see Prof . Reusch's further definition in the Notes ).
- The formation of the quinoline product is influenced by the interaction of both R group on the diketone and using methoxy-substituted anilines leads to the formation of 2-CF 3-quinolines.
- In addition to the rich chemistry of the Beirut reaction, Professor Haddadin did original work in the areas of Isobenzofuran, Isoindoles, tetrazines, quinolines, furans, pyrroles, cinnolines and indazoles.
- When the ?, ?-unsaturated carbonyl compound is prepared in situ from two carbonyl compounds ( via an Aldol condensation ), the reaction is known as the "'Beyer method for quinolines " '.
- Effective ( and efficient ) results can be obtained with an Ir ( I ) / phophinite / I 2 system and a Hantzsh ester-based organocatalytic system, both of which are similar to the systems discussed earlier with regards to quinolines.
- It's difficult to see quinolines in a sentence .
- The study concludes that the interaction of steric and electronic effects leads to the preferred formation of 2-CF 3-quinolines, which provides us with some information on how to manipulate the Combes quinoline synthesis to form a desired regioisomer as the product.
- These tautomerizations are represented in the images at right by the same process in closely related structures . ( The tautomerizations also take place when the adjacent all-carbon ring is absent . ) When represented as the carbonyl-containing tautomer often the most stable form, so the one observed in structure measurements such as room temperature NMR the pair of hydroxy-substitituted quinolines shown above are formally referred to as 2-quinolones ( oxygen adjacent to the ring N ) or 4-quinolones ( oxygen across from the ring N ), as the case may be.
Neighbors
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