The Use of Symmetry in Enantioselective Synthesis: Four Pairs of Chrysene Enantiomers Prepared from 19-Nortestosterone

Eva Stastna; Nigam P. Rath; Douglas F. Covey

doi:10.1039/c1ob05385j

The Use of Symmetry in Enantioselective Synthesis: Four Pairs of Chrysene Enantiomers Prepared from 19-Nortestosterone

Eva Stastna, Nigam P. Rath, Douglas F. Covey

University of Missouri-St. Louis

Research output: Contribution to journal › Article › peer-review

Original language	American English
Journal	Organic and Biomolecular Chemistry
Volume	9
DOIs	https://doi.org/10.1039/c1ob05385j
State	Published - Jan 1 2011

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Chemistry
Organic Chemistry

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10.1039/c1ob05385jLicense: Unspecified

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title = "The Use of Symmetry in Enantioselective Synthesis: Four Pairs of Chrysene Enantiomers Prepared from 19-Nortestosterone",

author = "Eva Stastna and Rath, \{Nigam P.\} and Covey, \{Douglas F.\}",

note = "Expansion of the D-ring of 19-norsteroids with incorporation of the steroid C-18 methyl group into a newly formed six-membered ring provides easy access to the chrysene ring system. By taking advantage of the symmetry of the chrysene ring system and avoiding ...",

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doi = "10.1039/c1ob05385j",

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T1 - The Use of Symmetry in Enantioselective Synthesis: Four Pairs of Chrysene Enantiomers Prepared from 19-Nortestosterone

AU - Stastna, Eva

AU - Rath, Nigam P.

AU - Covey, Douglas F.

N1 - Expansion of the D-ring of 19-norsteroids with incorporation of the steroid C-18 methyl group into a newly formed six-membered ring provides easy access to the chrysene ring system. By taking advantage of the symmetry of the chrysene ring system and avoiding ...

PY - 2011/1/1

Y1 - 2011/1/1

UR - https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3154374/

U2 - 10.1039/c1ob05385j

DO - 10.1039/c1ob05385j

M3 - Article

VL - 9

JO - Organic and Biomolecular Chemistry

JF - Organic and Biomolecular Chemistry

ER -

The Use of Symmetry in Enantioselective Synthesis: Four Pairs of Chrysene Enantiomers Prepared from 19-Nortestosterone

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