Syntheses of Post-Iboga Alkaloids

被引:9
作者
Lim, Hyeonggeun [1 ,2 ]
Seong, Sikwang [1 ,2 ]
Han, Sunkyu [1 ,2 ]
机构
[1] Korea Adv Inst Sci & Technol, Dept Chem, Daejeon 34141, South Korea
[2] Inst for Basic Sci Korea, Ctr Catalyt Hydrocarbon Functionalizat, Daejeon 34141, South Korea
来源
SYNTHESIS-STUTTGART | 2019年 / 51卷 / 14期
基金
新加坡国家研究基金会;
关键词
iboga alkaloids; post-iboga alkaloids; biosynthetic hypothesis; total synthesis; semi-synthesis; STEREOCONTROLLED TOTAL-SYNTHESIS; VINBLASTINE-VINCRISTINE SERIES; MONOTERPENOID INDOLE ALKALOIDS; ONE-POT SYNTHESIS; DIHYDROINDOLE ALKALOIDS; ENANTIOSELECTIVE SYNTHESES; BISINDOLE ALKALOIDS; ANTITUMOR ALKALOIDS; NATURAL-PRODUCTS; CATHARANTHINE;
D O I
10.1055/s-0037-1612061
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Post-iboga alkaloids are secondary metabolites that are biosynthetically derived from iboga-type alkaloids via rearrangements of the indole and/or isoquinuclidine moieties. Herein, we categorize post-iboga alkaloids into five types based on the biosynthetic mode of transformation of the iboga scaffold. We then describe reported syntheses of post-iboga alkaloids, including our laboratory's recent contributions, based on our own categorization. 1Introduction 1.1Iboga and Post-Iboga Alkaloids 1.2Classification of Post-Iboga Alkaloids 1.2.1Introduction to Type I Post-Iboga Alkaloids 1.2.2Introduction to Type II Post-Iboga Alkaloids 1.2.3Introduction to Type III Post-Iboga Alkaloids 1.2.4Introduction to Type IV Post-Iboga Alkaloids 1.2.5Introduction to Type V Post-Iboga Alkaloids 2Syntheses of Post-Iboga Alkaloids 2.1Syntheses of Type I Post-Iboga Alkaloids 2.1.1Syntheses of Monomeric Type I Post-Iboga Alkaloids 2.1.2Syntheses of Dimeric Type I Post-Iboga Alkaloids 2.2Syntheses of Type II Post-Iboga Alkaloids 2.3Synthetic Studies Toward Type III Post-Iboga Alkaloids 2.4Syntheses of Type IV Post-Iboga Alkaloids 2.5Synthesis of Type V Post-Iboga Alkaloids 3Conclusion and Outlook
引用
收藏
页码:2737 / 2758
页数:22
相关论文
共 95 条
[1]  
Alper K R, 2001, Alkaloids Chem Biol, V56, P1, DOI 10.1016/S0099-9598(01)56005-8
[2]   The ibogaine medical subculture [J].
Alper, Kenneth R. ;
Lotsof, Howard S. ;
Kaplan, Charles D. .
JOURNAL OF ETHNOPHARMACOLOGY, 2008, 115 (01) :9-24
[3]  
Alper KR, 1999, AM J ADDICTION, V8, P234
[4]   Enantioselective synthesis of cis- and trans-3,5-disubstituted piperidines.: Synthesis of 20S- and 20R-dihydrocleavamine [J].
Amat, M ;
Escolano, C ;
Lozano, O ;
Llor, N ;
Bosch, J .
ORGANIC LETTERS, 2003, 5 (17) :3139-3142
[5]   THE ALKALOIDS OF TABERNANTHE-IBOGA .4. THE STRUCTURES OF IBOGAMINE, IBOGAINE, TABERNANTHINE AND VOACANGINE [J].
BARTLETT, MF ;
DICKEL, DF ;
TAYLOR, WI .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1958, 80 (01) :126-136
[6]   A Straightforward Synthetic Entry to Cleavamine-Type Indole Alkaloids by a Ring-Closing Metathesis-Vinyl Halide Heck Cyclization Strategy [J].
Bennasar, M. -Lluisa ;
Sole, Daniel ;
Zulaica, Ester ;
Alonso, Sandra .
ORGANIC LETTERS, 2011, 13 (08) :2042-2045
[7]   A COMMON INTERMEDIATE PROVIDING SYNTHESES OF PSI-TABERSONINE, CORONARIDINE, IBOXYPHYLLINE, IBOPHYLLIDINE, VINAMIDINE, AND VINBLASTINE [J].
BORNMANN, WG ;
KUEHNE, ME .
JOURNAL OF ORGANIC CHEMISTRY, 1992, 57 (06) :1752-1760
[8]   VOACAMINE + VOACORINE [J].
BUCHI, G ;
MANNING, RE ;
MONTI, SA .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1964, 86 (21) :4631-&
[9]   TOTAL SYNTHESIS OF (+-)-IBOGAMINE AND OF (+-)-EPIIBOGAMINE [J].
BUCHI, G ;
COFFEN, DL ;
KOCSIS, K ;
SONNET, PE ;
ZIEGLER, FE .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1965, 87 (09) :2073-&
[10]   TOTAL SYNTHESIS OF IBOGA ALKALOIDS [J].
BUCHI, G ;
COFFEN, DL ;
KOCSIS, K ;
SONNET, PE ;
ZIEGLER, FE .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1966, 88 (13) :3099-&