Anodic cyclization reactions: the total synthesis of alliacol a.
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Synthetic Organic Electrochemistry: An Enabling and Innately Sustainable MethodAn expedient synthesis of a functionalized core structure of bielschowskysinTotal synthesis of dixiamycin B by electrochemical oxidationRecent Advances in the Stereoselective Synthesis of Tetrahydrofurans.Indole diterpenoid natural products as the inspiration for new synthetic methods and strategiesSynthetic Organic Electrochemical Methods Since 2000: On the Verge of a Renaissance.Appreciation of symmetry in natural product synthesis.Synthetic Organic Electrochemistry: Calling All Engineers.α-Carbonyl Cations in Sulfoxide-Driven Oxidative Cyclizations.Electrochemical synthesis of benzoxazoles from anilides - a new approach to employ amidyl radical intermediates.Total synthesis of hapalindole-type natural products.Flexible stereoselective functionalizations of ketones through umpolung with hypervalent iodine reagents.
P2860
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P2860
Anodic cyclization reactions: the total synthesis of alliacol a.
description
2003 nî lūn-bûn
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2003年の論文
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2003年学术文章
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name
Anodic cyclization reactions: the total synthesis of alliacol a.
@en
Anodic cyclization reactions: the total synthesis of alliacol a.
@nl
type
label
Anodic cyclization reactions: the total synthesis of alliacol a.
@en
Anodic cyclization reactions: the total synthesis of alliacol a.
@nl
prefLabel
Anodic cyclization reactions: the total synthesis of alliacol a.
@en
Anodic cyclization reactions: the total synthesis of alliacol a.
@nl
P356
P1476
Anodic cyclization reactions: the total synthesis of alliacol a.
@en
P2093
John Mihelcic
Kevin D Moeller
P356
10.1021/JA029064V
P407
P577
2003-01-01T00:00:00Z