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Journal of the American Chemical Society
|
December 1, 2005
Synthesis, structure, and reactivity of unexpectedly stable spiroepoxy-beta-lactones obtained by epoxidation of 4-alkylidene-2-oxetanones
Richard J Duffy, Kay A Morris, Daniel Romo
Organic Letters
|
August 14, 2010
Double diastereoselective, nucleophile-catalyzed aldol lactonizations (NCAL) leading to beta-lactone fused carbocycles and extensions to beta-lactone fused tetrahydrofurans
Kay A Morris, Kevin M Arendt, Seong Ho Oh, et al.
The Journal of Organic Chemistry
|
May 21, 2009
Asymmetric synthesis, structure, and reactivity of unexpectedly stable spiroepoxy-beta-lactones including facile conversion to tetronic acids: application to (+)-maculalactone A
Richard J Duffy, Kay A Morris, Ravikrishna Vallakati, et al.
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of 1
Search research articles
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Showing results (1-10 of 3) with videos related to
Sort By:
Page
of 1
Journal of the American Chemical Society
|
December 1, 2005
Synthesis, structure, and reactivity of unexpectedly stable spiroepoxy-beta-lactones obtained by epoxidation of 4-alkylidene-2-oxetanones
Richard J Duffy, Kay A Morris, Daniel Romo
Organic Letters
|
August 14, 2010
Double diastereoselective, nucleophile-catalyzed aldol lactonizations (NCAL) leading to beta-lactone fused carbocycles and extensions to beta-lactone fused tetrahydrofurans
Kay A Morris, Kevin M Arendt, Seong Ho Oh, et al.
The Journal of Organic Chemistry
|
May 21, 2009
Asymmetric synthesis, structure, and reactivity of unexpectedly stable spiroepoxy-beta-lactones including facile conversion to tetronic acids: application to (+)-maculalactone A
Richard J Duffy, Kay A Morris, Ravikrishna Vallakati, et al.
Page
of 1