Enantioselective construction of a polyhydroxylated pyrrolidine skeleton from 3-vinylaziridine-2-carboxylates: Synthesis of (+)-DMDP and a potential common intermediate for (+)-hyacinthacine A1 and (+)-1-epi-australine

Journal of Organic Chemistry

Volumn 77, Issue 18, 2012, Pages 7988-7999

  Kondo, Yukari ^a   Suzuki, Noriyuki ^a   Takahashi, Masato ^a   Kumamoto, Takuya ^a   Masu, Hyuma ^a   Ishikawa, Tsutomu ^a  

^a CHIBA UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

AZIRIDINATION; CYCLIZATION REACTIONS; DIASTEREO-SELECTIVITY; ENANTIOSELECTIVE CONSTRUCTION; ENANTIOSELECTIVE SYNTHESIS; GUANIDINIUM; HEATS OF FORMATION; PYRROLIDINES; PYRROLIZIDINE ALKALOID; STEREOSPECIFIC RING;

CARBOXYLATION; CYCLIZATION; ENANTIOSELECTIVITY; IODINE; IONIC LIQUIDS; METABOLITES; NITROGEN COMPOUNDS;

HYDROXYLATION;

1 EPI AUSTRALINE; 1,1 DIMETHYL 4 PHENYLPIPERAZINIUM; GUANIDINE; HYACINTHACINE A1; PYRROLIZIDINE ALKALOID; UNCLASSIFIED DRUG;

AMINATION; ARTICLE; CYCLIZATION; DRUG SYNTHESIS; ENANTIOSELECTIVITY; RING OPENING; STEREOCHEMISTRY; STEREOSPECIFICITY;

ALKALOIDS; CARBOXYLIC ACIDS; CYCLIZATION; MOLECULAR STRUCTURE; PYRROLIDINES; PYRROLIZIDINE ALKALOIDS; STEREOISOMERISM; VINYL COMPOUNDS;

EID: 84868118392     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo301178b     Document Type: Article

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