Synthesis of the guaianolide ring system via cycloaddition of a bicyclic carbonyl ylide with allyl propiolate.
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Formal synthesis of (-)-englerin A and cytotoxicity studies of truncated englerinsSynthesis and Biological Evaluation of New (-)-Englerin AnaloguesChemical synthesis of the englerins.Asymmetric Total Synthesis of (-)-Englerin A through Catalytic Diastereo- and Enantioselective Carbonyl Ylide Cycloaddition.Total synthesis and biological evaluation of (-)-englerin A and B: synthesis of analogues with improved activity profile.Chemical synthesis and biological evaluation of the englerin analogues.Collective total synthesis of englerin A and B, orientalol E and F, and oxyphyllol: application of the organocatalytic [4+3] cycloaddition reaction.A Double Allylation Strategy for Gram-Scale Guaianolide Production: Total Synthesis of (+)-Mikanokryptin.
P2860
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P2860
Synthesis of the guaianolide ring system via cycloaddition of a bicyclic carbonyl ylide with allyl propiolate.
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2010 nî lūn-bûn
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2010年の論文
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name
Synthesis of the guaianolide r ...... l ylide with allyl propiolate.
@en
Synthesis of the guaianolide r ...... l ylide with allyl propiolate.
@nl
type
label
Synthesis of the guaianolide r ...... l ylide with allyl propiolate.
@en
Synthesis of the guaianolide r ...... l ylide with allyl propiolate.
@nl
prefLabel
Synthesis of the guaianolide r ...... l ylide with allyl propiolate.
@en
Synthesis of the guaianolide r ...... l ylide with allyl propiolate.
@nl
P2093
P356
P1433
P1476
Synthesis of the guaianolide r ...... l ylide with allyl propiolate.
@en
P2093
Dmitry B Ushakov
H-Jürgen Meyer
Markus Ströbele
Martin E Maier
Vaidotas Navickas
P304
P356
10.1021/OL1012185
P407
P577
2010-08-01T00:00:00Z