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Intramolecular Cycloaddition Reactions of N-Acyl Imines. A Stereoselective Approach to the N-Terminal Amino Acid Component of Nikkomycin B
Michael J. Melnick
, Steven M. Weinreb
Chemistry
Research output
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Contribution to journal
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Article
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peer-review
43
Scopus citations
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Dive into the research topics of 'Intramolecular Cycloaddition Reactions of N-Acyl Imines. A Stereoselective Approach to the N-Terminal Amino Acid Component of Nikkomycin B'. Together they form a unique fingerprint.
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Keyphrases
Acyl
100%
Amino
25%
Amino Acid Complex
100%
Bicyclol
25%
Cyclization
25%
Cycloaddition
25%
Cycloaddition Reaction
100%
Cycloadducts
25%
Diels-Alder
50%
Glyoxylate
25%
Imines
100%
Intramolecular Cyclization
100%
Lactones
100%
Ring Cleavage
25%
Stereoselective Synthesis
25%
Stereoselectivity
100%
Chemistry
Amino Acid
100%
Carboxamide
25%
Diels-Alder Reaction
50%
Glyoxylate
25%
Imine
100%
Intramolecular Cycloaddition
100%
Lactone
100%
Nikkomycin
100%
Ring Cleavage
25%
Stereoselective Synthesis
25%