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Angewandte Chemie - International Edition

Volumn 50, Issue 34, 2011, Pages 7855-7857

Synthesis of oximidine II by a copper-mediated reductive ene-yne macrocyclization

(6) Schneider, Christopher M b Khownium, Kriangsak b Li, Wei c Spletstoser, Jared T b Haack, Torsten b Georg, Gunda I a

a UNIVERSITY OF MINNESOTA (United States)

b UNIVERSITY OF KANSAS (United States)

c UNIVERSITY OF MINNESOTA (United States)

Author keywords

anticancer agents; copper mediated reactions; macrocyclization; natural products; total synthesis

Indexed keywords

ANTI-CANCER AGENTS; COPPER-MEDIATED REACTIONS; MACRO-CYCLIZATION; NATURAL PRODUCTS; TOTAL SYNTHESIS;

COPPER; REACTION INTERMEDIATES;

SYNTHESIS (CHEMICAL);

ALKENE; ALKYNE; COPPER; LACTONE; ORGANOMETALLIC COMPOUND; OXIMIDINE II;

ARTICLE; CHEMICAL STRUCTURE; CHEMISTRY; CYCLIZATION; OXIDATION REDUCTION REACTION; STEREOISOMERISM; SYNTHESIS;

ALKENES; ALKYNES; CHEMISTRY TECHNIQUES, SYNTHETIC; COPPER; CYCLIZATION; LACTONES; MOLECULAR STRUCTURE; ORGANOMETALLIC COMPOUNDS; OXIDATION-REDUCTION; STEREOISOMERISM;

EID: 80051744706 PISSN: 14337851 EISSN: 15213773 Source Type: Journal
DOI: 10.1002/anie.201103081 Document Type: Article

Times cited : (15)

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