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Angewandte Chemie - International Edition

Volumn 52, Issue 49, 2013, Pages 13076-13079

Organoytterbium ate complexes extend the value of cyclobutenediones as isoprene equivalents

(5) Packard, Emma a Pascoe, David D a Maddaluno, Jacques b Gonçalves, Théo P a Harrowven, David C a

a UNIVERSITY OF SOUTHAMPTON (United Kingdom)

b UNIVERSITÉ DE ROUEN (France)

Author keywords

density functional calculations; flow chemistry; natural products; rearrangement; ytterbium

Indexed keywords

CHEMICAL REACTIONS; DENSITY FUNCTIONAL THEORY; YTTERBIUM;

COMPUTATIONAL STUDIES; CYCLOBUTENEDIONES; FLOW CHEMISTRY; GRIGNARD REAGENT; NATURAL PRODUCTS; ORGANOLITHIUMS; REARRANGEMENT; TOTAL SYNTHESIS;

CHEMISTRY;

1,3 BUTADIENE DERIVATIVE; BIOLOGICAL PRODUCT; CYCLOBUTANE DERIVATIVE; HEMITERPENE; HYDROQUINONE DERIVATIVE; ISOPRENE; KETONE; ORGANOMETALLIC COMPOUND; PENTANE; YTTERBIUM;

ARTICLE; CHEMICAL STRUCTURE; CHEMISTRY; DENSITY FUNCTIONAL CALCULATIONS; FLOW CHEMISTRY; NATURAL PRODUCTS; REARRANGEMENT; SYNTHESIS;

DENSITY FUNCTIONAL CALCULATIONS; FLOW CHEMISTRY; NATURAL PRODUCTS; REARRANGEMENT; YTTERBIUM;

BIOLOGICAL PRODUCTS; BUTADIENES; CYCLOBUTANES; HEMITERPENES; HYDROQUINONES; KETONES; MODELS, MOLECULAR; MOLECULAR STRUCTURE; ORGANOMETALLIC COMPOUNDS; PENTANES; YTTERBIUM;

EID: 84888583546 PISSN: 14337851 EISSN: 15213773 Source Type: Journal
DOI: 10.1002/anie.201307193 Document Type: Article

Times cited : (14)

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