机译:通过钾模板的非对映选择性的7- exo- Trig i>对抗致敏酮氨基醇的束缚氨基醇的循环加成循环加入的循环氨基醇与抗致剂活性
Department of Chemistry University of Kansas 1251 Wescoe Hall Drive Lawrence Kansas 66045-7582 United States;
Departments of Chemistry and Biology New Mexico Institute of Mining and Technology Socorro New Mexico 87801 United States;
Departments of Chemistry and Biology New Mexico Institute of Mining and Technology Socorro New Mexico 87801 United States;
Departments of Chemistry and Biology New Mexico Institute of Mining and Technology Socorro New Mexico 87801 United States;
Departments of Chemistry and Biology New Mexico Institute of Mining and Technology Socorro New Mexico 87801 United States;
Department of Chemistry University of Kansas 1251 Wescoe Hall Drive Lawrence Kansas 66045-7582 United States;
Department of Chemistry North Caucasus Federal University 1a Pushkin St. Stavropol 355009 Russian Federation;
Department of Chemistry University of Kansas 1251 Wescoe Hall Drive Lawrence Kansas 66045-7582 United States;
Department of Chemistry University of Kansas 1251 Wescoe Hall Drive Lawrence Kansas 66045-7582 United States;
机译:通过钾模板的非对映选择性的7- exo- Trig i>对抗致敏酮氨基醇的束缚氨基醇的循环加成循环加入的循环氨基醇与抗致剂活性
机译:2-氨基炔丙醇的非对映选择性合成。对映纯氨基γ-内酯和5-羟基哌啶酮衍生物的手性构件
机译:通过2-氮杂环丁酮系链的烯基醛的分子内硝酮-烯烃环加成反应生成新的稠合或桥连的三环β-内酰胺的非对映选择性路线-合成应用于咔唑和环状β-氨基酸衍生物
机译:通过拴系氨基醇的钾模板非对映选择性7-trio-trig环加成反应向对映纯的环丙烷融合的氧杂ze酮进行环丙烯的不对称化
机译:通过钾模板的氨基氨基醇的钾晶化氨基醇的钾型氨基醇的循环氨基醇与抗致剂活性的促进环丙烷 - 融合的恶己酮的去对称化