Regioselective Reductive Cross-Coupling Reactions of Unsymmetrical Alkynes

被引:91
作者
Reichard, Holly A. [1 ]
McLaughlin, Martin [1 ]
Chen, Ming Z. [1 ]
Micalizio, Glenn C. [1 ]
机构
[1] Scripps Res Inst, Dept Chem, Jupiter, FL 33458 USA
基金
美国国家卫生研究院;
关键词
Cross-coupling; Alkynes; Alkenes; Titanium; Synthetic methods; Reduction; Carbometalation; METAL-PROMOTED ALKYLATIONS; TITANOCENE-CATALYZED CYCLOCARBONYLATION; BOND-FORMING HYDROGENATION; IN-SITU GENERATION; STEREOSELECTIVE-SYNTHESIS; ALLYLIC ALCOHOLS; ALPHA; BETA-UNSATURATED ESTERS; DIASTEREOSELECTIVE SYNTHESIS; DIRECTED HYDROFORMYLATION; SPECTROSCOPIC PROPERTIES;
D O I
10.1002/ejoc.200901094
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The present Microreview summarizes our progress over the last few years in defining regioselective reductive cross-coupling reactions of unsymmetrical alkynes with terminal- and internal alkynes, aldehydes, and imines We begin with a brief historical perspective of metal-mediated reductive dimerization reactions of aromatic alkynes and discuss the challenges associated with "crossed" versions of this mode of reactivity Next, a collection of available methods that allow for regioselective reductive cross-coupling of internal alkynes with terminal and internal alkynes, aldehydes, and imines is summarized After an examination of the requirements for regioselectivity in these cases, the logic behind our design of alkoxide-directed titanium-mediated reductive cross-coupling reactions is presented A nomenclature is introduced to delineate the presumed mechanistic origin of regioselection associated with each reaction design, and a presentation of alkoxide-directed regioselective reductive cross-coupling reactions of alkynes follows Throughout, principal issues related to reactivity and selectivity are discussed to assess scope and limitations of available methods and to describe the broad challenges that exist for defining complex fragment union reactions based oil reductive cross-coupling chemistry
引用
收藏
页码:391 / 409
页数:19
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