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A convenient in situ procedure for effecting inter- and intramolecular Diels-Alder reactions of N-sulfonyl imines
Joseph Sisko, Steven M. Weinreb
Chemistry
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Article
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peer-review
75
Scopus citations
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Dive into the research topics of 'A convenient in situ procedure for effecting inter- and intramolecular Diels-Alder reactions of N-sulfonyl imines'. Together they form a unique fingerprint.
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Medicine & Life Sciences
boron trifluoride etherate
100%
Cycloaddition Reaction
71%
Imines
63%
Aldehydes
51%
Chemical Compounds
Diels-Alder Intramolecular Cycloaddition
55%
Boron Trifluoride
51%
Diels-Alder Reaction
41%
Imine
38%
Aldehyde
29%