Enantioselective Allylic Substitutions in Natural Product Synthesis

Enantioselective Allylic Substitutions in Natural Product Synthesis
复制标题

DOI:
10.1007/3418_2011_13
复制
发表时间:
2011
期刊:
ChemInform
影响因子:
--
通讯作者:
B. Trost;M. L. Crawley
B. Trost;M. L. Crawley
中科院分区:
其他
文献类型:
--
作者:
B. Trost;M. L. Crawley

文献摘要

被引文献

相似文献

对映选择性的过渡金属催化烯丙基取代反应构成了一个广泛而深入的方法,已扩大到包括更多的金属和配体。这些方法的实用性反映在广泛的天然产物和药物靶向全合成中,其将不对称烯丙基烷基化作为关键步骤。
Enantioselective transition metal-cataylzed allylic substitution reactions constitute a broad and deep methodology that has expanded to incorporate ever more metals and ligands. The utility of these processes is reflected in the wide range of natural product and drug target total syntheses that incorporate asymmetric allylic alkylations as the key step or steps.