A general method for the synthesis of bastaranes and isobastaranes: First total synthesis of bastadins 5, 10, 12, 16, 20, and 21

Chemistry - A European Journal

Volumn 11, Issue 1, 2005, Pages 406-421

  Couladouros, Elias A ^a,b   Pitsinos, Emmanuel N ^b   Moutsos, Vassilios I ^b   Sarakinos, Georgios ^b  

^a AGRICULTURAL UNIVERSITY OF ATHENS   (Greece)

^b INSTITUTE OF NANOSCIENCE AND NANOTECHNOLOGY   (Greece)

Author keywords

Diaryl ethers; Hypervalent compounds; Natural products; Oximino amides; Total synthesis

Indexed keywords

AMIDE BONDS; BASTARANES; BROMINATION; DIARYL ETHER FRAGMENTS;

CARBOXYLIC ACIDS; CHEMICAL BONDS; ETHERS; MOLECULAR DYNAMICS; NITROGEN COMPOUNDS;

SYNTHESIS (CHEMICAL);

AMIDE; BASTADIN; BASTADIN 10; BASTADIN 12; BASTADIN 16; BASTADIN 20; BASTADIN 21; BASTADIN 5; BASTARANE; DIAMINE; DICARBOXYLIC ACID; ETHER DERIVATIVE; ISOBASTARANE; NATURAL PRODUCT; UNCLASSIFIED DRUG;

ARTICLE; BROMINATION; CHEMICAL REACTION; CHEMICAL STRUCTURE; FOURIER TRANSFORMATION; INFRARED SPECTROSCOPY; MARINE ENVIRONMENT; MATRIX ASSISTED LASER DESORPTION IONIZATION TIME OF FLIGHT MASS SPECTROMETRY; NONHUMAN; PROTON NUCLEAR MAGNETIC RESONANCE; SPONGE (PORIFERA); SYNTHESIS;

BROMINE; COBALT; INDICATORS AND REAGENTS; LACTAMS; MODELS, MOLECULAR; MOLECULAR CONFORMATION; PHENYL ETHERS;

EID: 19944426067     PISSN: 09476539     EISSN: None     Source Type: Journal    
DOI: 10.1002/chem.200400904     Document Type: Article

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