Recent progress in the synthesis of heterocyclic natural products by the Staudinger/intramolecular aza-Wittig reaction

Arkivoc

Volumn 2005, Issue 2, 2005, Pages 98-99

  Eguchi, Shoji ^a  

^a NAGOYA UNIVERSITY   (Japan)

Author keywords

Alkaloids; Antibiotics; Aza Wittig reaction; Benzodiazepine; Eguchi aza Wittig protocol; Iminophosphorane; Polymer supported Eguchi protocol; Quinazolinone annelation; Tandem intramolecular Staudinger aza Wittig reaction

Indexed keywords

1,2,3,11A TETRAHYDRO 8 HYDROXY 7 METHOXY 5H PYRROLO[2,1 C][1,4]BENZODIAZEPIN 5 ONE; 5 N ACETYLARDEEMIN; ALKALOID DERIVATIVE; ANHYDRONUPHARAMINE; ANTHRAMYCIN; ANTIBIOTIC AGENT; ARDEEMIN; ASPERLICIN; ASPERLICIN C; BENZODIAZEPINE DERIVATIVE; BENZOMALVIN A; BENZOMALVIN B; CHOLECYSTOKININ RECEPTOR BLOCKING AGENT; CIRCUMDATIN F; CRYPTOTACKIENE; DENDROBINE; FUMIQUINAZOLINE F; FUMIQUINAZOLINE G; GLOMERINE; GLYANTRYPINE; IMINE; LY 411575; NATURAL PRODUCT; QUINAZOLINONE DERIVATIVE; RUTAECARPINE; SCLEROTIGENIN; TACHYKININ RECEPTOR ANTAGONIST; TRYPTANTHRIN; UNCLASSIFIED DRUG; UNINDEXED DRUG; VASCINE; VASICINONE;

CYCLIZATION; DRUG DESIGN; DRUG SYNTHESIS; METHODOLOGY; REVIEW; STAUDINGER REACTION; WITTIG REACTION;

EID: 17844376761     PISSN: 14246376     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review

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