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Volumn 23, Issue 18, 2013, Pages 5192-5194
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A new strategy for the synthesis of crucigasterin A, and cytotoxic activity of this compound and its related analogues
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Author keywords
Chelation controlled; Crucigasterin A; Cytotoxicity; Grignard addition; Julia olefination; Total synthesis
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Indexed keywords
ANTINEOPLASTIC AGENT;
CRUCIGASTERIN A;
MALIC ACID;
NATURAL PRODUCT;
UNCLASSIFIED DRUG;
ANTINEOPLASTIC ACTIVITY;
ARTICLE;
ASCIDIACEA;
BIRCH REDUCTION;
BREAST ADENOCARCINOMA;
CANCER CELL CULTURE;
CHELATION;
CONTROLLED STUDY;
DRUG ISOLATION;
DRUG STRUCTURE;
DRUG SYNTHESIS;
HUMAN;
HUMAN CELL;
IN VITRO STUDY;
OLEFINATION;
PSEUDODISTOMA CRUCIGASTER;
STEREOCHEMISTRY;
SWERN OXIDATION;
UTERINE CERVIX CANCER;
CHELATION CONTROLLED GRIGNARD ADDITION;
CRUCIGASTERIN A;
CYTOTOXICITY;
JULIA OLEFINATION;
TOTAL SYNTHESIS;
AMINO ALCOHOLS;
ANTINEOPLASTIC AGENTS;
CELL LINE, TUMOR;
CELL PROLIFERATION;
DOSE-RESPONSE RELATIONSHIP, DRUG;
DRUG SCREENING ASSAYS, ANTITUMOR;
HELA CELLS;
HUMANS;
MCF-7 CELLS;
MOLECULAR STRUCTURE;
STRUCTURE-ACTIVITY RELATIONSHIP;
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EID: 84882623692
PISSN: 0960894X
EISSN: 14643405
Source Type: Journal
DOI: 10.1016/j.bmcl.2013.07.007 Document Type: Article |
Times cited : (6)
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References (31)
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