A synthetic sequence was developed in which a diene containing an attached secondary amine was reacted with maleic anhydride to afford the title structures in one step. The reaction involves a Diels-Alder reaction combined with a transacylation reaction of the imide group. A series of six scaffolds was constructed using this methodology. Each scaffold was subsequently reacted with 12 amines to afford a library containing 72 compounds.
Synthesis of N-Alkyl-octahydroisoquinolin-1-one-8-carboxamide Libraries Using a Tandem Diels-Alder/Acylation Sequence. Publishing Authors By Initials
Synthesis of N-Alkyl-octahydroisoquinolin-1-one-8-carboxamide Libraries Using a Tandem Diels-Alder/Acylation Sequence. Journal Published:
PUBLICATION TYPE: Journal Article
Journal: Journal of combinatorial chemistry
VOLUME: 9
Page Numbers: 1188-92
Journal Abbreviation:
ISSN: 1520-4766
DAY: 27
MONTH: 09
YEAR: 2007
Synthesis of N-Alkyl-octahydroisoquinolin-1-one-8-carboxamide Libraries Using a Tandem Diels-Alder/Acylation Sequence. Information
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LANGUAGE: eng
NlmUniqueID: 100886263
Synthesis of N-Alkyl-octahydroisoquinolin-1-one-8-carboxamide Libraries Using a Tandem Diels-Alder/Acylation Sequence. Keywords Mesh Terms:
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Grant and Affiliation Information for Synthesis of N-Alkyl-octahydroisoquinolin-1-one-8-carboxamide Libraries Using a Tandem Diels-Alder/Acylation Sequence.
AFFILIATION: jaube@ku.edu.
Country: United States
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MEDLINETA: J Comb Chem
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