An Enantioselective Synthesis of the ABD Tricycle for (-)-Phomactin A Featuring Rawal's Asymmetric Diels-Alder Cycloaddition.
about
Synthesis of tetrasubstituted 1-silyloxy-3-aminobutadienes and chemistry beyond Diels-Alder reactionsA macrocyclic β-iodoallenolate intermediate is key: synthesis of the ABD core of phomactin A.Cascade cyclizations of acyclic and macrocyclic alkynones: studies toward the synthesis of phomactin A.Total synthesis of (±)-phomactin A. Lessons learned from respecting a challenging structural topology.Total synthesis of phomactin A.Constructing the Architecturally Distinctive ABD-Tricycle of Phomactin A through an Intramolecular Oxa-[3 + 3] Annulation Strategy.
P2860
An Enantioselective Synthesis of the ABD Tricycle for (-)-Phomactin A Featuring Rawal's Asymmetric Diels-Alder Cycloaddition.
description
2008 nî lūn-bûn
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2008年の論文
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2008年学术文章
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name
An Enantioselective Synthesis ...... ric Diels-Alder Cycloaddition.
@en
An Enantioselective Synthesis of the ABD Tricycle for
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type
label
An Enantioselective Synthesis ...... ric Diels-Alder Cycloaddition.
@en
An Enantioselective Synthesis of the ABD Tricycle for
@nl
prefLabel
An Enantioselective Synthesis ...... ric Diels-Alder Cycloaddition.
@en
An Enantioselective Synthesis of the ABD Tricycle for
@nl
P2093
P2860
P356
P1476
An Enantioselective Synthesis ...... ric Diels-Alder Cycloaddition.
@en
P2093
Aaron A Bedermann
Aleksey V Kurdyumov
Grant S Buchanan
Kevin P Cole
Ling-Feng You
Richard P Hsung
P2860
P304
P356
10.1002/ADSC.200800552
P577
2008-12-01T00:00:00Z