Copper-catalyzed multi-component reactions synthesis of nitrogen-containing polycyclic compounds /

A 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 byproduct. Based on this reaction, a copper-catalyzed synthesis of...

Full description

Main Author: Ohta, Yusuke.
Other Authors: SpringerLink (Online service)
Format: eBook
Language: English
Published: Berlin ; Heidelberg ; New York : Springer, ©2011.
Berlin ; Heidelberg ; New York : [2011]
Physical Description: 1 online resource (xv, 102 pages).
Series: Springer theses.
Subjects:
LEADER 05683cam a2200973 a 4500
001 704393945
003 OCoLC
005 20240223121953.0
006 m o d
007 cr cn|||||||||
008 110301s2011 gw obm 000 0 eng d
010 |a 2010938324 
019 |a 701369181  |a 771448118  |a 779852404  |a 1005787031  |a 1162647805  |a 1391808568 
020 |a 9783642154737  |q (electronic bk.) 
020 |a 3642154735  |q (electronic bk.) 
020 |a 3642154727 
020 |a 9783642154720 
020 |z 9783642154720 
035 |a (OCoLC)704393945  |z (OCoLC)701369181  |z (OCoLC)771448118  |z (OCoLC)779852404  |z (OCoLC)1005787031  |z (OCoLC)1162647805  |z (OCoLC)1391808568 
037 |a 978-3-642-15472-0  |b Springer  |n http://www.springerlink.com 
040 |a GW5XE  |b eng  |e pn  |c GW5XE  |d EBLCP  |d YDXCP  |d OCLCQ  |d MHW  |d OCLCQ  |d QE2  |d N$T  |d OCLCQ  |d OCLCO  |d OCLCF  |d BEDGE  |d OCLCQ  |d COO  |d DEBSZ  |d OCLCQ  |d ESU  |d VT2  |d OCLCQ  |d IOG  |d CEF  |d U3W  |d AU@  |d YOU  |d OCLCQ  |d OCLCO  |d OL$  |d OCLCQ  |d OCLCO  |d OCL  |d OCLCQ  |d AJS  |d OCLCQ  |d COM  |d OCLCO  |d OCLCQ  |d AUD  |d OCLCO  |d OCLCL 
049 |a COM6 
050 4 |a QD401  |b .O38 2011 
072 7 |a SCI  |x 013040  |2 bisacsh 
082 0 4 |a 547/.2  |2 22 
100 1 |a Ohta, Yusuke. 
245 1 0 |a Copper-catalyzed multi-component reactions :  |b synthesis of nitrogen-containing polycyclic compounds /  |c Yusuke Ohta. 
260 |a Berlin ;  |a Heidelberg ;  |a New York :  |b Springer,  |c ©2011. 
264 1 |a Berlin ;  |a Heidelberg ;  |a New York :  |b Springer,  |c [2011] 
264 4 |c ©2011. 
300 |a 1 online resource (xv, 102 pages). 
336 |a text  |b txt  |2 rdacontent. 
337 |a computer  |b c  |2 rdamedia. 
338 |a online resource  |b cr  |2 rdacarrier. 
490 1 |a Springer theses. 
502 |b Ph. D.  |c Kyoto University  |d 2010. 
504 |a Includes bibliographical references. 
520 |a A 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 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. Following these results, extensive application studies using one-pot palladium-, acid-, or base-promoted cyclization revealed that indole- or isoquinoline. 
588 0 |a Print version record. 
505 0 |a Copper-Catalyzed Multi-Component Reactions; Supervisor's Foreword; Acknowledgments; Contents; 1 Introduction; References; Part I Synthesis of Indole Derivatives; 2 Construction of 2-(Aminomethyl)indoles Through Copper-Catalyzed Domino Three-Component Coupling and Cyclization; 3 Facile Synthesis of 1,2,3,4-Tetrahydro- beta -Carbolines by One-Pot Domino Three-Component Indole Formation and Nucleophilic Cyclization; 4 Concise Synthesis of Indole-Fused 1,4-Diazepines through Copper(I)-Catalyzed Domino Three-Component Coupling-Cyclization-N-Arylation under Microwave Irradiation. 
505 8 |a Part II Synthesis of Isoquinoline Derivatives5 Facile Synthesis of 3-(Aminomethyl)isoquinoline by Copper-Catalyzed Domino Four-Component Coupling and Cyclization; 6 Rapid Access to 3-(Aminomethyl)isoquinoline-Fused Polycyclic Compounds by Copper-Catalyzed Four Component Coupling, Cascade Cyclization, and Oxidation; 7 Conclusions. 
506 |a University staff and students only. Requires University Computer Account login off-campus. 
650 0 |a Polycyclic compounds  |x Synthesis. 
650 6 |a Composés polycycliques  |x Synthèse. 
650 7 |a SCIENCE  |x Chemistry  |x Organic.  |2 bisacsh. 
650 7 |a Chimie.  |2 eclas. 
650 7 |a Science des matériaux.  |2 eclas. 
650 7 |a Polycyclic compounds  |x Synthesis.  |2 fast. 
655 2 |a Academic Dissertation. 
655 7 |a dissertations.  |2 aat. 
655 7 |a Academic theses.  |2 fast. 
655 7 |a Academic theses.  |2 lcgft. 
655 7 |a Thèses et écrits académiques.  |2 rvmgf. 
710 2 |a SpringerLink (Online service) 
776 0 8 |i Print version:  |a Ohta, Yusuke.  |t Copper-catalyzed multi-component reactions.  |d Berlin ; Heidelberg ; New York : Springer, ©2011  |z 9783642154720  |w (OCoLC)704393945. 
830 0 |a Springer theses. 
907 |a .b32878229  |b multi  |c -  |d 110408  |e 240320 
998 |a (3)cue  |a cu  |b 240227  |c m  |d z   |e -  |f eng  |g gw   |h 0  |i 2 
948 |a MARCIVE Overnight, in 2024.03 
948 |a MARCIVE Comp, in 2022.12 
948 |a MARCIVE Comp, 09/2021 
948 |a MARCIVE Over, 07/2021 
948 |a MARCIVE Comp, 2019.12 
948 |a MARCIVE Comp, 2018.05 
948 |a MARCIVE August, 2017 
948 |a MARCIVE extract Aug 5, 2017 
994 |a 92  |b COM 
995 |a Loaded with m2btab.ltiac in 2024.03 
995 |a Loaded with m2btab.elec in 2024.02 
995 |a Loaded with m2btab.ltiac in 2022.12 
995 |a Loaded with m2btab.ltiac in 2021.09 
995 |a Loaded with m2btab.ltiac in 2021.07 
995 |a Loaded with m2btab.elec in 2021.06 
995 |a Loaded with m2btab.ltiac in 2019.12 
995 |a Loaded with m2btab.ltiac in 2018.06 
995 |a Loaded with m2btab.ltiac in 2017.08 
995 |a Loaded with m2btab.ltiac in 2017.08 
995 |a Loaded with m2btab.ltiac in 2017.08 
995 |a Loaded with m2btab.elec in 2016 
995 |a Loaded with m2btab.elec in 2016 
995 |a OCLC offline update by CMU 
999 |e z 
999 |a cue 
989 |d cueme  |e  - -   |f  - -   |g -   |h 0  |i 0  |j 200  |k 240227  |l $0.00  |m    |n  - -   |o -  |p 0  |q 0  |t 0  |x 0  |w SpringerLink  |1 .i150273022  |u http://ezproxy.coloradomesa.edu/login?url=https://link.springer.com/10.1007/978-3-642-15473-7  |3 SpringerLink  |z Click here for access