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標(biāo)題: Titlebook: Copper-Catalyzed Multi-Component Reactions; Synthesis of Nitroge Yusuke Ohta Book 2011 Springer-Verlag Berlin Heidelberg 2011 atom economy. [打印本頁]

作者: 加冕    時間: 2025-3-21 16:37
書目名稱Copper-Catalyzed Multi-Component Reactions影響因子(影響力)




書目名稱Copper-Catalyzed Multi-Component Reactions影響因子(影響力)學(xué)科排名




書目名稱Copper-Catalyzed Multi-Component Reactions網(wǎng)絡(luò)公開度




書目名稱Copper-Catalyzed Multi-Component Reactions網(wǎng)絡(luò)公開度學(xué)科排名




書目名稱Copper-Catalyzed Multi-Component Reactions被引頻次




書目名稱Copper-Catalyzed Multi-Component Reactions被引頻次學(xué)科排名




書目名稱Copper-Catalyzed Multi-Component Reactions年度引用




書目名稱Copper-Catalyzed Multi-Component Reactions年度引用學(xué)科排名




書目名稱Copper-Catalyzed Multi-Component Reactions讀者反饋




書目名稱Copper-Catalyzed Multi-Component Reactions讀者反饋學(xué)科排名





作者: Integrate    時間: 2025-3-21 21:10
Conclusions,nnich-type reaction using 2-ethynylanilines, aldehydes, and secondary amines, followed by hydroamination. This is the first example of three-component indole formation without producing any salts as a byproduct. Using alkyl aldehydes and the chiral ligand PINAP, the corresponding indole bearing a br
作者: 鉆孔    時間: 2025-3-22 01:27

作者: 說笑    時間: 2025-3-22 08:35

作者: decode    時間: 2025-3-22 09:54

作者: NICHE    時間: 2025-3-22 13:09

作者: NICHE    時間: 2025-3-22 20:40
2190-5053 of many readers..This research is the first example of a thrA copper-catalyzed direct synthesis of 2-(aminomethyl)indoles by catalytic domino reaction including multi-component coupling was developed, and is the first example of a three-component indole formation without producing salts as a byprodu
作者: 功多汁水    時間: 2025-3-22 23:38
Identifying the needs of a target groupanched substituent was produced with moderate ee values. This indole formation was applicable to the synthesis of indole-fused polycyclic compounds via palladium-catalyzed C–H functionalization at 3-position of indole. Synthetic application to calindol, benzo[.][1,2]thiazines, and indene was also conducted.
作者: Baffle    時間: 2025-3-23 03:46

作者: 大看臺    時間: 2025-3-23 05:55

作者: 臭了生氣    時間: 2025-3-23 10:06

作者: Cpap155    時間: 2025-3-23 16:40
Conclusions,anched substituent was produced with moderate ee values. This indole formation was applicable to the synthesis of indole-fused polycyclic compounds via palladium-catalyzed C–H functionalization at 3-position of indole. Synthetic application to calindol, benzo[.][1,2]thiazines, and indene was also conducted.
作者: bifurcate    時間: 2025-3-23 18:41
Construction of 2-(Aminomethyl)indoles Through Copper-Catalyzed Domino Three-Component Coupling and g this domino reaction and C–H functionalization at the indole C-3 position, polycyclic indoles were readily synthesized. Construction of benzo[e][1,2]thiazine and indene motifs by the reaction of sulfonamide and malonate congeners is also presented.
作者: orthopedist    時間: 2025-3-24 02:04

作者: 發(fā)誓放棄    時間: 2025-3-24 04:57
Book 2011e first example of a three-component indole formation without producing salts as a byproduct. Based on this reaction, a copper-catalyzed synthesis of 3-(aminomethyl)isoquinoline was accomplished which represents an unprecedented isoquinoline synthesis through a four-component coupling reaction. Foll
作者: Jejune    時間: 2025-3-24 08:37

作者: Consensus    時間: 2025-3-24 13:14
Facile Synthesis of 1,2,3,4-Tetrahydro-β-Carbolines by One-Pot Domino Three-Component Indole Formatiino three-component coupling-cyclization using an appropriate ethynylaniline, aldehyde, and a secondary amine, treatment with .-BuOK/hexane or MsOH afforded the desired tetrahydro-β-carboline derivatives in moderate to good yields.
作者: APEX    時間: 2025-3-24 15:59

作者: Infinitesimal    時間: 2025-3-24 19:13

作者: 傻    時間: 2025-3-24 23:57
Copper-Catalyzed Multi-Component Reactions978-3-642-15473-7Series ISSN 2190-5053 Series E-ISSN 2190-5061
作者: Exclude    時間: 2025-3-25 04:00
Identifying the needs of a target groupino three-component coupling-cyclization using an appropriate ethynylaniline, aldehyde, and a secondary amine, treatment with .-BuOK/hexane or MsOH afforded the desired tetrahydro-β-carboline derivatives in moderate to good yields.
作者: indoctrinate    時間: 2025-3-25 11:16
Identifying the needs of a target groupeloped. Treatment of 2-ethynylbenzaldehydes with paraformaldehyde, secondary amine, and .-BuNH. in the presence of a catalytic amount of CuI in DMF affords 3-(aminomethyl)isoquinolines in good yields, through successive formation of one carbon–carbon and three carbon–nitrogen bonds.
作者: 里程碑    時間: 2025-3-25 13:43
Evaluating the outcomes of a group programmeon, has been developed. A Mannich-type reaction with 2-ethynylbenzaldehyde, paraformaldehyde, and a secondary amine followed by treatment with a diamine component gave tricyclic isoquinolines through cascade cyclization and oxidation. Construction of fused isoquinolines of various ring sizes is also presented.
作者: innovation    時間: 2025-3-25 18:07
Identifying the needs of a target groupures found in bioactive compounds, natural products, and so on. It is also important to effectively utilize the limited carbon resources minimizing the requisite reagents, solvents, cost, time, separation processes, and wastes [., .]. The multi-component reaction (MCR) [.–.], represented by Ugi’s fo
作者: tenosynovitis    時間: 2025-3-25 22:02
Identifying the needs of a target groupnnich-type reaction using 2-ethynylanilines, aldehydes, and secondary amines, followed by hydroamination. This is the first example of three-component indole formation without producing any salts as a byproduct. Using alkyl aldehydes and the chiral ligand PINAP, the corresponding indole bearing a br
作者: Anticlimax    時間: 2025-3-26 02:25

作者: Eclampsia    時間: 2025-3-26 05:00
Identifying the needs of a target groupino three-component coupling-cyclization using an appropriate ethynylaniline, aldehyde, and a secondary amine, treatment with .-BuOK/hexane or MsOH afforded the desired tetrahydro-β-carboline derivatives in moderate to good yields.
作者: senile-dementia    時間: 2025-3-26 09:08

作者: Inelasticity    時間: 2025-3-26 13:53

作者: 流動性    時間: 2025-3-26 18:56
Yusuke OhtaNominated by the University of Kyoto (Pharmaceutical Sciences), Japan for a Springer.The work of the thesis will inspire synthetic research of many readers..This research is the first example of a thr
作者: paltry    時間: 2025-3-26 21:06

作者: 一起    時間: 2025-3-27 02:41

作者: 人類學(xué)家    時間: 2025-3-27 06:51

作者: 增減字母法    時間: 2025-3-27 12:11
https://doi.org/10.1007/978-3-642-15473-7atom economy; bioactive compounds; complex heterocyclic structures; copper salt; green chemistry; indole
作者: 得罪    時間: 2025-3-27 13:50

作者: 共和國    時間: 2025-3-27 20:46
Book 1914 sind. Der Verlag stellt mit diesem Archiv Quellen für die historische wie auch die disziplingeschichtliche Forschung zur Verfügung, die jeweils im historischen Kontext betrachtet werden müssen. Dieser Titel erschien in der Zeit vor 1945 und wird daher in seiner zeittypischen politisch-ideologischen Ausrichtung vom Verlag nicht beworben.




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