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Volumn 9, Issue 21, 2011, Pages 7372-7383
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Diastereoselective one-pot Wittig olefination-Michael addition and olefin cross metathesis strategy for total synthesis of cytotoxic natural product (+)-varitriol and its higher analogues
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Author keywords
[No Author keywords available]
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Indexed keywords
CYTOTOXIC;
D-RIBOSE;
DIASTEREOSELECTIVE;
DRUG DEVELOPMENT;
KEY FEATURE;
MARINE NATURAL PRODUCTS;
NATURAL PRODUCTS;
OLEFIN CROSS-METATHESIS;
ONE POT;
OXA-MICHAEL ADDITION;
STEREO-SELECTIVE;
STRUCTURAL FEATURE;
SYNTHETIC APPROACH;
SYNTHETIC STRATEGIES;
TOTAL SYNTHESIS;
WITTIG OLEFINATION;
ADDITION REACTIONS;
CYTOTOXICITY;
OLEFINS;
STEREOSELECTIVITY;
SYNTHESIS (CHEMICAL);
ALKENE;
ANTINEOPLASTIC AGENT;
BENZYL ALCOHOL DERIVATIVE;
BIOLOGICAL PRODUCT;
FURAN DERIVATIVE;
VARITRIOL;
ANIMAL;
ARTICLE;
CELL PROLIFERATION;
CELL STRAIN 3T3;
CELL STRAIN HL 60;
CHEMISTRY;
CONFORMATION;
DRUG EFFECT;
DRUG SCREENING;
HUMAN;
MOUSE;
STEREOISOMERISM;
STRUCTURE ACTIVITY RELATION;
SYNTHESIS;
TUMOR CELL LINE;
ALKENES;
ANIMALS;
ANTINEOPLASTIC AGENTS;
BENZYL ALCOHOLS;
BIOLOGICAL AGENTS;
CELL LINE, TUMOR;
CELL PROLIFERATION;
DRUG SCREENING ASSAYS, ANTITUMOR;
FURANS;
HL-60 CELLS;
HUMANS;
MICE;
MOLECULAR CONFORMATION;
NIH 3T3 CELLS;
STEREOISOMERISM;
STRUCTURE-ACTIVITY RELATIONSHIP;
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EID: 80053939702
PISSN: 14770520
EISSN: None
Source Type: Journal
DOI: 10.1039/c1ob06039b Document Type: Article |
Times cited : (36)
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References (40)
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