简单吲哚生物碱以及具有未重排单萜单元的生物碱。 - Suppr

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Simple indole alkaloids and those with a nonrearranged monoterpenoid unit.

作者信息

Hibino S, Choshi T

机构信息

Faculty of Pharmacy and Pharmaceutical Sciences, Fukuyama University, Hiroshima, Japan.

出版信息

Nat Prod Rep. 2001 Feb;18(1):66-87. doi: 10.1039/b004055j.

DOI:10.1039/b004055j

PMID:11245401

Abstract

摘要

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Simple indole alkaloids and those with a nonrearranged monoterpenoid unit.

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Simple indole alkaloids and those with a nonrearranged monoterpenoid unit.

作者信息

Hibino S, Choshi T

机构信息

Faculty of Pharmacy and Pharmaceutical Sciences, Fukuyama University, Hiroshima, Japan.

出版信息

Nat Prod Rep. 2001 Feb;18(1):66-87. doi: 10.1039/b004055j.

DOI:10.1039/b004055j

PMID:11245401

Abstract

摘要

相似文献

Simple indole alkaloids and those with a nonrearranged monoterpenoid unit.

Nat Prod Rep. 2001 Feb;18(1):66-87. doi: 10.1039/b004055j.

Simple indole alkaloids and those with a nonrearranged monoterpenoid unit.

Nat Prod Rep. 2000 Apr;17(2):175-91. doi: 10.1039/a809402k.

Simple indole alkaloids and those with a nonrearranged monoterpenoid unit.

Nat Prod Rep. 2003 Apr;20(2):216-42. doi: 10.1039/b110074m.

Simple indole alkaloids and those with a nonrearranged monoterpenoid unit.

Nat Prod Rep. 2002 Apr;19(2):148-80. doi: 10.1039/b007740m.

Recent progress in the chemistry of the monoterpenoid indole alkaloids.

Nat Prod Rep. 1995 Aug;12(4):385-411. doi: 10.1039/np9951200385.

Simple indole alkaloids and those with a non-rearranged monoterpenoid unit.

Nat Prod Rep. 2005 Feb;22(1):73-103. doi: 10.1039/b316241a. Epub 2005 Jan 10.

Simple indole alkaloids and those with a nonrearranged monoterpenoid unit.

Nat Prod Rep. 2005 Dec;22(6):761-93. doi: 10.1039/b502162f. Epub 2005 Nov 11.

Simple indole alkaloids and those with a nonrearranged monoterpenoid unit.

Nat Prod Rep. 2007 Aug;24(4):843-68. doi: 10.1039/b516351j. Epub 2007 Mar 23.

Simple indole alkaloids and those with a nonrearranged monoterpenoid unit.

Nat Prod Rep. 2015 Sep 23;32(10):1389-471. doi: 10.1039/c5np00032g.

Chemistry and biology of new marine alkaloids from the indole and annelated indole series.

Curr Med Chem. 2003 Jul;10(13):1113-27. doi: 10.2174/0929867033457511.

引用本文的文献

Unexplored Facet of Pincer Ligands: Super-Reductant Behavior Applied to Transition-Metal-Free Catalysis.

JACS Au. 2023 Apr 10;3(4):1213-1220. doi: 10.1021/jacsau.3c00077. eCollection 2023 Apr 24.

Organocatalysed one-pot three component synthesis of 3,3'-disubstituted oxindoles featuring an all-carbon quaternary center and spiro[2-pyran-3,4'-indoline].

RSC Adv. 2023 Apr 28;13(19):13206-13212. doi: 10.1039/d3ra00510k. eCollection 2023 Apr 24.

Mutagenesis Reveals That the Gene Is Required for Enhancing the Alkaline Tolerance in Rice.

Front Plant Sci. 2019 Jun 11;10:759. doi: 10.3389/fpls.2019.00759. eCollection 2019.

Alcohols as Substrates and Solvents for the Construction of 3-Alkoxylated-2-Oxindoles by Direct Alkoxylation of 3-Halooxindoles.

Molecules. 2017 May 13;22(5):801. doi: 10.3390/molecules22050801.

A new approach for the synthesis of bisindoles through AgOTf as catalyst.

Beilstein J Org Chem. 2014 Sep 17;10:2206-14. doi: 10.3762/bjoc.10.228. eCollection 2014.

RuCl₃·3H₂O catalyzed reactions: facile synthesis of bis(indolyl)methanes under mild conditions.

Molecules. 2011 May 9;16(5):3855-68. doi: 10.3390/molecules16053855.

One-pot synthesis of polysubstituted indoles from aliphatic nitro compounds under mild conditions.

Tetrahedron Lett. 2007 Mar 5;48(10):1809-1811. doi: 10.1016/j.tetlet.2007.01.031.