Definition, Meaning & Anagrams | English word ENANTIOPURE


ENANTIOPURE

Definitions of ENANTIOPURE

  1. Enantiomerically pure (containing a single enantiomer).

1

Number of letters

11

Is palindrome

No

19
AN
ANT
EN
ENA
IO
IOP
NA
NAN
NT
OP
PU
PUR
RE

AE
AEO
AER
AET
AI
AIE

Examples of Using ENANTIOPURE in a Sentence

  • Chiral pool synthesis is used to build a part of epothilone (an alternative to paclitaxel) from readily available enantiopure (–)-pantolactone.
  • the specific rotation of enantiopure 1-phenylethanol can be enhanced by the addition of achiral acetophenone as an impurity.
  • Homochirality can also refer to enantiopure substances in which all the constituents are the same enantiomer (a right-handed or left-handed version of an atom or molecule), but some sources discourage this use of the term.
  • A partly enantiopure variant of allethrin I, consisting of only two stereoisomers in an approximate ratio of 1:1, is called bioallethrin.
  • Chemically, armodafinil is the enantiopure (R)-(–)-enantiomer of the racemic mixture modafinil (brand name Provigil).
  • For example, an enantiopure poly (isocyanate) derivative has been shown to form ordered arrays of squashed donut structures.
  • Even for a product which can be attained through an asymmetric catalytic or auxiliary-based route, the racemate may be significantly less expensive than the enantiopure material, resulting in heightened cost-effectiveness even with the inherent "loss" of 50% of the material.
  • Originally synthesized in 1993, several groups have designed novel and creative methods of synthesizing enantiopure solenopsin and other alkaloidal components of ant venom.
  • These diastereomers may be separated by column chromatography and hydrolyzed to obtain each enantiomer of Pirkle's alcohol in enantiopure form.
  • Levoamphetamine was first introduced in the form of racemic amphetamine under the brand name Benzedrine in 1935 and as an enantiopure drug under the brand name Cydril in the 1970s.
  • Enantiopure tert-butanesulfinamide can be prepared by enantioselective oxidation of inexpensive di-tert-butyl disulfide to the thiosulfinate followed by disulfide bond cleavage by lithium amide.
  • Enantiopure p-toluene-sulfinyl imines arise by the reaction of the commercially available Andersen reagent (menthyl p-toluenesulfinate) with metallo-ketimines but is limited to ketone derived N-sulfinyl imines.
  • After treatment of stannatrane chloride with lithium napthalide, a lithium carbastannatrane was quenched with the corresponding enantiopure mesylate to yield the desired enantioenriched alkyl carbastannatrane in moderate yield with high enantiomeric excess.
  • The derived chiral imine is used to prepare enantiopure α-trifluoromethyl alanines and diamines by a Strecker reaction followed by either nitrile hydrolysis or reduction.
  • Indirect enantiomer separation involves the interaction between the chiral analyte (CA) of interest and the suitable reactive CS (in this case it is an enantiopure chiral derivatizing agent, CDA) leading to the formation of a covalent diastereomeric complex that can be separated with an achiral chromatographic technique.
  • from Freie Universität Berlin in Synthetic Organic Chemistry (New transformations of enantiopure 3,6-dihydro-2H-1,2-oxazines ring cleavages, ring enlargements and a novel approach to carbohydrate mimetics) in 2005.
  • Over the years, the Couty's azetidine synthesis was shown to be efficient to access a variety of enantiopure azetidines and 2-cyano-azetidines were shown to be excellent scaffolds and building blocks in heterocyclic chemistry and for molecular diversity.



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