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A racemic mixture is an optically inactive mixture of equal amounts of two enantiomers. If your product is achiral, then there are no enantiomers ...
pubs.rsc.org/en/content/articlelanding/2000/mc/x0010083
The conditions required for resolving racemates into enantiomers by crystallization involve a deficiency of either the conglomerator or the achiral solubiliser to ...
Enantioselective synthesis - Wikipedia, the free encyclopedia
en.wikipedia.org/wiki/Enantioselective_synthesis
Chiral pool synthesis is the easiest approach: A chiral starting material is manipulated through successive reactions using achiral reagents that retain its chirality ...
dx.doi.org/10.1021/ja903371d
Jun 22, 2009 ... Nuclear Magnetic Resonance Signaling of Molecular Chiral Information Using an Achiral Reagent. Abstract; HTML Full Text HTML; PDF Hi-Res ...
www.sciencedirect.com/science/article/pii/0960894X95003... www.sciencedirect.com/science/article/pii/0960894X9500315K
The synthesis of a new functionalized achiral linker reagent (10) for the incorporation of multiple primary amino groups into oligonucleotides is described .
www.ncbi.nlm.nih.gov/pubmed/19545158
Jul 15, 2009 ... Nuclear magnetic resonance signaling of molecular chiral information using an achiral reagent. Shundo A, Labuta J, Hill JP, Ishihara S, Ariga K ...
www.mendeley.com/research/resolution-racemates-achiral-... www.mendeley.com/research/resolution-racemates-achiral-reagents/
(2000) Kostyanovsky et al. Mendeleev Communications. Read by researchers in: 100% Chemistry. Type: journal. Volume: 10. Pages: 83-84. ISSN: 09599436.
academics.keene.edu/rblatchly/OrgoCommon/hand/stereoche... academics.keene.edu/rblatchly/OrgoCommon/hand/stereochem/chiralrxns.html
Only one stereogenic center involved; achiral reagents, etc.: If an existing stereogenic center is not involved in the reaction, there will be no change in the ...
crab.rutgers.edu/~burke/organic/Ch05Su08.doc
Achiral objects have mirror images that are identical to the object. ..... of an optically active reagent or catalyst to convert an achiral reactant into a chiral product.
www.organic-chemistry.org/abstracts/lit2/007.shtm
(BDP)CuH: A “Hot” Stryker's Reagent for Use in Achiral Conjugate Reductions. Benjamin A. Baker, Žarko V. Bošković and Bruce H. Lipshutz*. *Department of ...
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