Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About
0 | 1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | a | b | c | d | e | f | g | h | i | j | k | l | m | n | o | p | q | r | s | t | u | v | w | x | y | z

   |<      <<      >>     > |    


Kerr-effect functions, calculated from induced tRpole reorientation alone for disc-like ones

Kerr-effect reorientation functions for dgar-shaped microsystems below it lie the continuous-line curves — ly for disc-like

Kerr-McGee Corporation uranium Kerr-McGee Corporation.

Kestose . intramolecular

Kesuhs for mica surfaces approaching irt potassium chloride solution.

Ketal 65 and ketone 67 formation via ring contractions

Ketal and glycoside synthesis.

Ketal hydrolysis overview. The most likely reaction path is boxed.

Ketalized compounds from moraceous plants

KETALIZED DIELS-ALDER-TYPE ADDUCTS

Ketals II and III obtained through the intramolecular cyclization of 8a,17-epoxy-14,15-dinorlabdan-13-one I.

Ketamine has many names, both for the drug itself and for the experience of taking the drug. These are some of the most popular street terms for ketamine and its use.

Ketamine is sold for veterinary use in liquid form under the brand name Ketaset . Because drug abusers know ketamine is readily available in veterinary clinics, this may put animal health professionals at risk for attack or burglary by people who want to obtain the otherwise illegal drug.

Ketamine release from the multiple emulsion with shearing.

Ketamine was originally used in both humans and animals as an anesthetic during surgery. Vials containing the liquid form of ketamine, like the ones pictured here, are still widely used for veterinary purposes.

Ketamine-based inactivation of 1 -aminocyciopropane-1 -carboxylate synthase by AVG.

Ketcha-Gribble synthesis of ellipticine quinone 33 and ellipticine .

Ketcha-Gribble synthesis of isoellipticine quinone 36 and isoellipticine .

Ketde heated with steam or hot water .

Ketene dimerisation catalysed by TB fSO-QN.

Ketene formation by alkyne oxidation with rhodium catalysis.

Ketene formation by cobalt ll -porphyrin catalysed carbene carbonylation. Reprinted from Ref. 41 with permission from Wiiey VCH.

Ketene formation by cyclopropenone ring opening. H

Ketene formation from alkyne oxidation with a ruthenium catalyst.

Ketene formation from malonic acid.



   |<      <<      >>     > |    

SEARCH



© 2024 chempedia.info