Simple indole alkaloids and those with a non-rearranged monoterpenoid unit.
about
Inhibitory effects of caffeine analogues on neoplastic transformation: structure-activity relationship.Synthesis and preliminary biological studies of 3-substituted indoles accessed by a palladium-catalyzed enantioselective alkene difunctionalization reaction.Palladium-catalyzed dynamic kinetic asymmetric transformations of vinyl aziridines with nitrogen heterocycles: rapid access to biologically active pyrroles and indoles.Identification of small-molecule enhancers of arginine methylation catalyzed by coactivator-associated arginine methyltransferase 1.C2-Alkylation of N-pyrimidylindole with vinylsilane via cobalt-catalyzed C-H bond activation.Lewis Acid Mediated Vinylogous Additions of Enol Nucleophiles into an α,β-Unsaturated Platinum CarbenePalladium-catalyzed enantioselective C-3 allylation of 3-substituted-1H-indoles using trialkylboranes.Microwave-assisted synthesis of 5,6-dihydroindolo[1,2-a]quinoxaline derivatives through copper-catalyzed intramolecular N-arylation.Studies on the alkaloids of the calycanthaceae and their syntheses.Biomimetic Total Syntheses of (-)-Leucoridines A and C through the Dimerization of (-)-DihydrovalparicineA tandem isomerization/prins strategy: iridium(III)/Brønsted acid cooperative catalysisTriflic acid controlled successive annelation of aromatic sulfonamides: An efficient one-pot synthesis of N-sulfonyl pyrroles, indoles and carbazolesA sequential metal-catalyzed C-N bond formation in the synthesis of 2-amido-indoles.Ni(NHC)]-catalyzed cycloaddition of diynes and tropone: apparent enone cycloaddition involving an 8π insertion.Highly diastereoselective samarium diiodide induced cyclizations of new 3-substituted indole derivatives.Vinylation of nitro-substituted indoles, quinolinones, and anilides with grignard reagents.Indole synthesis by rhodium(III)-catalyzed hydrazine-directed C-H activation: redox-neutral and traceless by N-N bond cleavage.Preparation of functionalized indoles and azaindoles by the intramolecular copper-mediated carbomagnesiation of ynamides.Microwave-accelerated Pd-catalyzed desulfitative direct C2-arylation of free (NH)-indoles with arylsulfinic acids.Cobalt-catalysed reductive C-H alkylation of indoles using carboxylic acids and molecular hydrogen.Dehydrogenation of secondary amines: synthesis, and characterization of rare-earth metal complexes incorporating imino- or amido-functionalized pyrrolyl ligands.Intramolecular Cooperative CC Bond Cleavage Reaction of 1,3-Dicarbonyl Compounds with 2-Iodoanilines to Give o-(N-Acylamino)aryl Ketones and Multisubstituted Indoles.Pd-catalyzed regioselective intramolecular direct arylation of 3-indolecarboxamides: access to spiro-indoline-3,3'-oxindoles and 5,11-dihydro-6H-indolo[3,2-c]quinolin-6-ones.Palladium-catalyzed regioselective C-H fluoroalkylation of indoles at the C4-position.Palladium-Catalyzed Intramolecular Trost-Oppolzer-Type Alder-Ene Reaction of Dienyl Acetates to Cyclopentadienes.Polycyclization Enabled by Relay Catalysis: One-Pot Manganese-Catalyzed C-H Allylation and Silver-Catalyzed Povarov Reaction.Cobalt(III)-Catalyzed Redox-Neutral Synthesis of Unprotected Indoles Featuring an N-N Bond Cleavage.Indole Synthesis through Sequential Electrophilic N-H and C-H Bond Activation Using Iodine(III) Reactivity.Palladium-catalyzed oxidative arylacetoxylation of alkenes: synthesis of indole and indoline derivatives.One-pot synthesis of 2,3-difunctionalized indoles via Rh(iii)-catalyzed carbenoid insertion C-H activation/cyclization.Design of Organic Transformations at Ambient Conditions: Our Sincere Efforts to the Cause of Green Chemistry Practice.Highly enantioselective yttrium(III)-catalyzed Friedel-Crafts alkylation of β-trichloro(trifluoro)methyl aryl enones with indoles.Efficient Friedel-Crafts alkylation of indoles and pyrrole with enones and nitroalkene in water.One-pot relay catalysis: divergent synthesis of furo[3,4-b]indoles and cyclopenta[b]indoles from 3-(2-aminophenyl)-1,4-enynols.Synthesis of N-vinylindoles through copper catalyzed cyclization reaction of N-(2-alkynylphenyl)imine.Silver triflate catalyzed tandem heterocyclization/alkynylation of 1-((2-tosylamino)aryl)but-2-yne-1,4-diols to 2-alkynyl indoles.Mild and efficient C2-alkenylation of indoles with alkynes catalyzed by a cobalt complex.I2-mediated regioselective C-3 azidation of indoles.A density functional theory study of the mechanism of isomerization of 2-aryl-2H-azirines to 2,3-disubstituted indoles by FeCl2 and Rh2(O2CCF3)4.Towards the core structure of Strychnos alkaloids using samarium diiodide-induced reactions of indole derivatives.
P2860
Q33696709-439340E9-E7BB-4786-B90C-8951A922EDBFQ33960977-D1007920-46D9-40DE-85B2-315D5613FBB5Q34287188-520D9F7D-3756-4753-8B09-DA0D78AE0EDBQ34456824-C9F52E37-6C44-48C0-9473-4C66E976C9FFQ36281221-B6A62137-6E8A-4176-AC52-C33F7D8BDA02Q36520367-3C6A317A-7DDE-46B8-BED3-872837F3EE89Q36837325-FDBF4985-AB6F-400F-A2E9-73D1465CED2AQ37406237-A5706844-A76E-4C3E-9BF9-8462AF3D0CB8Q38425885-2855B369-7BA9-435C-94F1-2F7C932E2F8AQ41020714-492BFAAF-03F8-46BD-914B-5FBE0352E66AQ41898587-703A1FBB-A256-4D40-97F0-B9DBA80C10FBQ41909934-717F65AC-F05F-4687-9BD5-0B62C592D4FFQ42265424-DA41521D-7B0F-4C3C-A384-91EE3895EE73Q42553483-86034D40-835A-4B06-98AA-CC68394C4667Q43261154-6D6F219D-37A8-43C6-9072-EEE753234CECQ43278151-2AB3DBFC-05CC-4E56-897D-885DC0D4E98FQ43450381-4DF56970-715D-44B6-85E8-4067A33E7DA9Q44744907-299B4B88-2A98-401C-A33A-AEBA61036B91Q44885991-A81C6AB5-CB31-46BA-B1C3-30BA22C00716Q45784235-7C0EC266-8B9B-4662-B786-135EAECCA1A4Q46303625-8DAFC9FE-3E42-4301-958E-B91B05552D47Q46733831-81907871-6C33-443D-8C2A-A719C0948F24Q47983460-07A54AE6-8AB1-44F8-BF54-7C428CDE4CC5Q48132804-5E84F1C8-ED45-461C-A83D-94D2F2C1AE84Q48153533-FE784F6C-2213-445D-85D8-03EB047B5298Q48191916-CE2061B0-4599-4663-9322-A4BD7FD71371Q48248981-167ED31D-8E1E-4A65-9810-1B3E0C7AEC73Q48276975-10BE0802-2124-4D74-B47F-175E4CE1F05AQ49686840-ED18EF54-1018-4A1E-8986-2C33D9A34AC6Q50120349-9B48051E-D7AC-4918-8694-E7F5ED16F740Q50239124-33FEC8E8-EA90-4028-B7A3-7FAC970D4BB3Q50519121-569D9D78-AA83-4B0C-B604-E194CD41DD8BQ50708197-4F62CC9E-7A80-4CCE-9B44-98E9DCF4791AQ50873492-B79D8926-B498-48E3-86DA-C4C7D4611BC7Q50969812-CC338537-74CA-4B98-82F4-D66C34409A33Q51379539-F1E40F29-8DC4-4AB5-A489-5397F30DE1B4Q51388598-DE7B919B-F1C2-4DD4-A2E2-A5F9248063D2Q51497030-D79CE67E-641A-4A66-A312-F9885FB681ABQ51753616-25E29FDB-1F0C-4E9B-B7DB-6CF6E1FF0218Q52881689-65E17010-4419-4E1F-9DC1-CF54C22FFFCF
P2860
Simple indole alkaloids and those with a non-rearranged monoterpenoid unit.
description
2005 nî lūn-bûn
@nan
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
2005年论文
@zh
2005年论文
@zh-cn
name
Simple indole alkaloids and those with a non-rearranged monoterpenoid unit.
@ast
Simple indole alkaloids and those with a non-rearranged monoterpenoid unit.
@en
type
label
Simple indole alkaloids and those with a non-rearranged monoterpenoid unit.
@ast
Simple indole alkaloids and those with a non-rearranged monoterpenoid unit.
@en
prefLabel
Simple indole alkaloids and those with a non-rearranged monoterpenoid unit.
@ast
Simple indole alkaloids and those with a non-rearranged monoterpenoid unit.
@en
P356
P1476
Simple indole alkaloids and those with a non-rearranged monoterpenoid unit.
@en
P2093
Fumio Yamada
Masanori Somei
P304
P356
10.1039/B316241A
P577
2005-01-10T00:00:00Z