Examples of 'wittig' in a sentence
Meaning of "wittig"
wittig (adjective) - relating to or characteristic of German chemist Georg Wittig, known for his work on organic synthesis involving the Wittig reaction
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- A surname.
How to use "wittig" in a sentence
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wittig
Wittig reaction pathways will be discussed first.
It is also a precursor to more elaborated Wittig reagents.
Wittig homologation introduces the side chain.
Writings by others include writings about Wittig.
Wittig reactions also provide the styrylpyridine compounds.
Differences of reactivity are also noted in Wittig reactions.
Wittig was a theorist of material feminism.
This reaction is well known as Wittig reaction.
Wittig reaction which is well known to those skilled in the art.
Styrylthiophenes can also be prepared vÃa the Wittig reaction.
A Wittig reaction may be used to convert a ketone or an aldehyde to an alkene.
The stage is now wet for intramolecular Wittig reaction.
The Wittig reagent is prepared by known art recognized procedures.
The corresponding reaction involving an ether is the Wittig rearrangement.
The Wittig reaction leads to the retinoic acid ester.
See also
Numerous organic chemistry textbooks describe the Wittig reaction.
A Wittig reagent can be used to form an alkene from an aldehyde.
Nalmefene can be produced from naltrexone by the Wittig reaction.
Wittig pointed to an upcoming Quartet meeting as a possible indicator on the situation.
This result is ascribed to steric inhibition of the intramolecular Wittig reaction.
The Wittig reaction can also be performed in the opposite direction.
This may be carried out using normal Wittig reaction conditions.
The Wittig reaction is carried out in a solvent such as dichloromethane at ambient temperature.
That a weaker base could be used in a Wittig reaction is indeed surprising.
The Wittig reaction provided herein is applicable to many isoprene unit precursors.
Ii further processing of naltrexone obtained from i to nalmefene optionally by the Wittig reaction.
The procedure in the Wittig reaction can be divided into two steps.
Identification of the acyclic intermediates was necessary to understand the mechanism of these Wittig reactions.
Processes for carrying out Wittig reactions are extensively described in the literature.
This synthetic pathway begins in a manner similar to the Wittig reaction pathway of FIG.
The Wittig reaction is known as an exceedingly useful method for the synthesis of alkenes.
Conditions for carrying out a Wittig reaction are known to those skilled in the art.
This step can be carried out according to a usual method of the Wittig reaction.
The Wittig reaction is effected repeatedly or combined with another kind of the Wittig reaction.
This aldehyde was used without purification and isolation in a Wittig reaction described as follows.
A final Wittig reaction was utilized to incorporate the glycine moiety and complete the skeleton.
The general working conditions are those recommended in the technique for Wittig reactions.
The Wittig olefination reaction is well known and commonly employed by the skilled artisan.
Commercially available cyclic ether ketones can be reacted in a Wittig reaction to produce olefinesters.
Addition of the Wittig Reagent from triethylphosphono acetate to cyclohexanone to give ethyl cyclohexylidene acetate.
These are conveniently combined with triphenylphosphine in a suitable solvent to form the reactive Wittig salts.
The Wittig reaction is a popular method for the synthesis of alkene from ketones and aldehydes.
The product is dried in a vacum oven and used directly in the next Wittig reaction.
As above the Wittig reaction is employed using the known appropriately substituted heterocyclic aldehyde derivatives.
This reaction may be carried out in accordance with a conventional manner of the Wittig reaction.
Monique Wittig imagines gender as class.
Vedejs has put forth a theory to explain the stereoselectivity of stabilized and unstabilized Wittig reactions.
I always saw Sintolt and Wittig only at enmity.
This reaction may be carried out in accordance with a conventional manner for the Wittig reaction.
This ylide undergoes a Wittig Reaction when exposed to an aldehyde.
