1,4-Diazaspiro[2.2]pentanes as a flexible platform for the synthesis of diamine-bearing stereotriads

Journal of Organic Chemistry

Volumn 77, Issue 5, 2012, Pages 2446-2455

  Rigoli, Jared W ^a   Boralsky, Luke A ^a   Hershberger, John C ^a   Marston, Dagmara ^a   Meis, Alan R ^a   Guzei, Ilia A ^a   Schomaker, Jennifer M ^a  

^a UNIVERSITY OF WISCONSIN MADISON   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALTERNATIVE APPROACH; AZIRIDINES; BIOLOGICALLY ACTIVE COMPOUNDS; CARBON-HETEROATOM BONDS; FLEXIBLE PLATFORMS; HETEROATOMS; PROPARGYL ALCOHOL; REGIOSELECTIVE RING OPENING; RING OPENING; RING OPENING REACTION;

BIOACTIVITY; OLEFINS; PARAFFINS; REACTION INTERMEDIATES; SCAFFOLDS;

ORGANIC COMPOUNDS;

1,4 DIAZASPIRO[2.2]PENTANE; ALLENE DERIVATIVE; AZIRIDINE DERIVATIVE; DIAMINE; NUCLEOPHILE; PENTANE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL BOND; CHEMICAL REACTION; CHIRALITY; CRYSTAL STRUCTURE; STEREOISOMERISM; SYNTHESIS;

DIAMINES; MOLECULAR STRUCTURE; SPIRO COMPOUNDS; STEREOISOMERISM;

EID: 84857809944     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo3000282     Document Type: Article

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