LICP OpenIR  > 羰基合成与选择氧化国家重点实验室(OSSO)
Enantioselective Total Synthesis of (-)-Walsucochin B
DepartmentOSSO国家重点实验室
Xu, Shiyan1; Gu, Jixiang1; Li HL(李辉林)1; Ma, Donghui1; Xie XG(谢新刚)1; She XG(厍学功)1,2; Xie XG(谢新刚); She XG(厍学功)
2014
Source PublicationOrganic Letters
ISSN1523-7060
Volume16Issue:7Pages:1996-1999
Abstract

The first enantioselective total synthesis of the structurally unique nortriterpenoid (−)-walsucochin B has been accomplished through the cationic polyolefin cyclization initiated by chiral epoxide. The core framework and the stereocenters in the natural product were all constructed in this step. A site-selective, late-stage free-radical halogenation and Seyferth–Gilbert homologation was adopted to install the acetylene moiety to synthesize the phenylacetylene. The absolute configuration of walsucochin B was confirmed through enantioselective total synthesis.

Subject Area物理化学与绿色催化
DOI10.1021/ol500553x
Funding Organizationthe NSFC (21125207;21102062;21372103);the MOST (2010CB833203);PCSIRT (IRT1138);the FRFCU (lzujbky-2013-49;lzujbky-2013-ct02);Program 111
Indexed BySCI
If6.364
Language英语
compositor第二作者单位
Citation statistics
Cited Times:29[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://ir.licp.cn/handle/362003/21250
Collection羰基合成与选择氧化国家重点实验室(OSSO)
Corresponding AuthorXie XG(谢新刚); She XG(厍学功)
Affiliation1.Lanzhou Univ, Coll Chem & Chem Engn, State Key Lab Appl Organ Chem, Lanzhou 730000, Peoples R China
2.Chinese Acad Sci, Lanzhou Inst Chem Phys, State Key Lab Oxo Synth & Select Oxidat, Lanzhou 730000, Peoples R China
Recommended Citation
GB/T 7714
Xu, Shiyan,Gu, Jixiang,Li HL,et al. Enantioselective Total Synthesis of (-)-Walsucochin B[J]. Organic Letters,2014,16(7):1996-1999.
APA Xu, Shiyan.,Gu, Jixiang.,Li HL.,Ma, Donghui.,Xie XG.,...&厍学功.(2014).Enantioselective Total Synthesis of (-)-Walsucochin B.Organic Letters,16(7),1996-1999.
MLA Xu, Shiyan,et al."Enantioselective Total Synthesis of (-)-Walsucochin B".Organic Letters 16.7(2014):1996-1999.
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