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Angewandte Chemie - International Edition

Volumn 51, Issue 37, 2012, Pages 9288-9291

Chemical synthesis of aspidosperma alkaloids inspired by the reverse of the biosynthesis of the rhazinilam family of natural products

(3) McMurray, Lindsay a Beck, Elizabeth M a Gaunt, Matthew J a

a UNIVERSITY OF CAMBRIDGE (United Kingdom)

Author keywords

biomimetic synthesis; C H functionalization; domino reactions; natural products; reduction

Indexed keywords

ASPIDOSPERMA; BIOMIMETIC SYNTHESIS; C-H FUNCTIONALIZATION; CASCADE PROCESS; CHEMICAL SYNTHESIS; DOMINO REACTIONS; NATURAL PRODUCTS; PYRROLE DERIVATIVES; SECONDARY METABOLITES;

AROMATIC COMPOUNDS; BIOCHEMISTRY; BIOMIMETICS; NITROGEN COMPOUNDS; REACTION KINETICS; REDUCTION;

METABOLITES;

ALKALOID; ASPIDOSPERMIDINE; BIOLOGICAL PRODUCT; CARBON; HYDROGEN; INDOLE ALKALOID; INDOLIZINE DERIVATIVE; LACTAM; METAL; PYRROLE DERIVATIVE; QUINOLINE DERIVATIVE; RHAZINILAM;

ARTICLE; ASPIDOSPERMA; BIOSYNTHESIS; CATALYSIS; CHEMISTRY; CYCLIZATION; METABOLISM; OXIDATION REDUCTION REACTION; SYNTHESIS;

ALKALOIDS; ASPIDOSPERMA; BIOLOGICAL AGENTS; CARBON; CATALYSIS; CYCLIZATION; HYDROGEN; INDOLE ALKALOIDS; INDOLIZINES; LACTAMS; METALS; OXIDATION-REDUCTION; PYRROLES; QUINOLINES;

EID: 84865848799 PISSN: 14337851 EISSN: 15213773 Source Type: Journal
DOI: 10.1002/anie.201204151 Document Type: Article

Times cited : (66)

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