Intramolecular 1,3-dipolar cycloaddition-mediated stereoselective synthesis of disubstituted cyclopentane: A simple model for the cyclopentane ring system of polycyclic oroidine alkaloids

Chemistry - An Asian Journal

Volumn 8, Issue 1, 2013, Pages 244-250

  Fukahori, Yusuke ^a   Takayama, Yohei ^a   Imaoka, Takuya ^a   Iwamoto, Osamu ^a   Nagasawa, Kazuo ^a  

^a TOKYO UNIVERSITY OF AGRICULTURE AND TECHNOLOGY   (Japan)

Author keywords

axinellamine; cycloaddition; guanidine; oroidine; redox chemistry

Indexed keywords

CYCLOADDITION; REDOX REACTIONS; STEREOCHEMISTRY;

1 ,3-DIPOLARCYCLOADDITION; AXINELLAMINE; DIASTEREOSELECTIVE SYNTHESIS; GUANIDINE; INTRAMOLECULAR REDOX REACTIONS; OROIDINE; REDOX CHEMISTRY; STEREOSELECTIVE SYNTHESIS;

STEREOSELECTIVITY;

ALKALOID; CYCLOPENTANE DERIVATIVE; POLYCYCLIC HYDROCARBON;

ARTICLE; CHEMICAL STRUCTURE; CHEMISTRY; CYCLOADDITION; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; STEREOISOMERISM; SYNTHESIS;

ALKALOIDS; CYCLOADDITION REACTION; CYCLOPENTANES; MAGNETIC RESONANCE SPECTROSCOPY; MODELS, MOLECULAR; POLYCYCLIC COMPOUNDS; STEREOISOMERISM;

MLCS; MLOWN;

EID: 84871563058     PISSN: 18614728     EISSN: 1861471X     Source Type: Journal    
DOI: 10.1002/asia.201200820     Document Type: Article

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