Asymmetric addition to chiral aromatic and unsaturated oxazolines using a novel chiral auxillary

DOI: 10.1055/s-1993-25842

Source and publish data:

Synthesis p. 250 - 262 (1993)

Update date:2022-08-04

Topics:

Authors:

Meyers Meyers

Schmidt Schmidt

McKennon

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Article abstract of DOI:10.1055/s-1993-25842

By utilizing S-serine, both enantiomers of the reduced methoxyamino alcohol (12) were efficiently prepared. The corresponding oxazolines, prepared from these auxiliaries, showed favorable properties toward additions to naphthalenes 22 and cyclohexene, 27.

Full text of DOI:10.1055/s-1993-25842

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Article Doi

Asymmetric addition to chiral aromatic and unsaturated oxazolines using a novel chiral auxillary

DOI: 10.1055/s-1993-25842

Source and publish data:

Authors:

Article abstract of DOI:10.1055/s-1993-25842

Full text of DOI:10.1055/s-1993-25842

Products guided by the article

R&D Labs maybe for 1019020-13-3

Relevant to this article

Subtle balance of steric and electronic effects for the synthesis of atactic polyketones catalyzed by Pd complexes with meta-substituted Aryl-BIAN ligands

Inert Carbon Free Radicals. 7. "The (Kinetic) Reverse Effect" and Relevant Synthesis of New Monofunctionalized Triphenylmethyl Radicals and Their Nonradical Counterparts

Transformation of alkynyl sulfones into alkynylphosphonates with trialkyl phosphites

Cesium fluoride and tetra-n-butylammonium fluoride mediated 1,4-N→O shift of disubstituted phenyl ring of a bicalutamide derivative

Practical synthesis of a vanilloid receptor-1 antagonist

The syntheses of potential medicinal agents from 1-methyl-3-bromo-3-piperidyl phenyl ketone.