Synthetic approach toward α-aminomethyl-γ-butyrolactones from β-lactam synthons elaborated by SmI2-mediated reductive coupling reactions

Natural Product Communications

Volumn 8, Issue 7, 2013, Pages 889-896

  Takahashi, Masaki ^a   Sudo, Takahiro ^a   Murata, Yusuke ^a   Sengoku, Tetsuya ^a   Yoda, Hidemi ^a  

^a SHIZUOKA UNIVERSITY   (Japan)

Author keywords

Successive ring opening and lactonization; aminomethyl butyrolactone; lactam synthon

Indexed keywords

ALANTOLACTONE; ALPHA AMINOMETHYL GAMMA BUTYROLACTONE DERIVATIVE; AMBROSIN; BETA LACTAM DERIVATIVE; COSTUNOLIDE; GAMMA BUTYROLACTONE DERIVATIVE; HELENALIN; PARTHENOLIDE; SAMARIUM DIIODIDE; SAUSSUREAMINE A; SAUSSUREAMINE B; SAUSSUREAMINE C; SAUSSUREAMINE D; SAUSSUREAMINE E; SINULAMINE I; SINULAMINE II; SINULAMINE III; UNCLASSIFIED DRUG;

ARTICLE; CONTROLLED STUDY; DRUG SYNTHESIS; LACTONIZATION; REDUCTION; RING OPENING;

EID: 84880812209     PISSN: 1934578X     EISSN: 15559475     Source Type: Journal    
DOI: 10.1177/1934578x1300800709     Document Type: Article

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