Znn3bq.jpeg
²é¿´: 238  |  »Ø¸´: 2
±¾Ìû²úÉú 1 ¸ö £¬µã»÷ÕâÀï½øÐв鿴
µ±Ç°Ö»ÏÔʾÂú×ãÖ¸¶¨Ìõ¼þµÄ»ØÌû£¬µã»÷ÕâÀï²é¿´±¾»°ÌâµÄËùÓлØÌû

412003280

ľ³æ (Ö°Òµ×÷¼Ò)

[ÇóÖú] ÇóÖúһƪÎÄÕµÄAccession number£¿

ÇóÖúÎÄÕµÄAccession number£¿


ÎÄÕÂÐÅÏ¢
ÌâÄ¿£ºPalladium-Catalyzed Nucleophilic Substitution/C¨CH Activation/Aromatization Cascade Reaction: One Approach To Construct 6-Unsubstituted Phenanthridines
doi£º10.1021/acs.joc.5b02145
Á¬½Ó£ºhttps://pubs.acs.org/doi/abs/10.1021/acs.joc.5b02145

» ²ÂÄãϲ»¶

ÌìÌì°áש
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû

°¢´ô´ô´ô

Ìú¸Ëľ³æ (ÖªÃû×÷¼Ò)

‡å‡å³æ

¡¾´ð°¸¡¿Ó¦Öú»ØÌû

¡ï ¡ï ¡ï ¡ï ¡ï
412003280: ½ð±Ò+5, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, Ëٶȷdz£¿ì£¬Ð»Ð» 2016-03-05 18:31:41
Ðľ²_ÒÀÈ»: LS-EPI+1, ¸ÐлӦÖú 2016-03-05 18:40:46
Accession number:       
20154801620710
        Title:        Palladium-Catalyzed Nucleophilic Substitution/C-H Activation/Aromatization Cascade Reaction: One Approach to Construct 6-Unsubstituted Phenanthridines
        Authors:         Han, Wenyong1 Email author hanwy@zmc.edu.cn; Zhou, Xiaojian1; Yang, Siyi1; Xiang, Guangyan1; Cui, Baodong1; Chen, Yongzheng1 Email author yzchen@zmc.edu.cn
        Author affiliation:        1 School of Pharmacy, Zunyi Medical University, Zunyi, China
        Corresponding author:         Han, Wenyong (hanwy@zmc.edu.cn)
        Source title:        Journal of Organic Chemistry
        Abbreviated source title:        J. Org. Chem.
        Volume:        80
        Issue:        22
        Issue date:        November 20, 2015
        Publication year:        2015
        Pages:        11580-11587
        Language:        English
        ISSN:         00223263
        E-ISSN:         15206904
        CODEN:         JOCEAH
        Document type:        Journal article (JA)
        Publisher:        American Chemical Society
        Abstract:        A facile and practical palladium-catalyzed nucleophilic substitution/C-H activation/aromatization cascade reaction has been developed. A range of 6-unsubstituted phenanthridines could be obtained in moderate to good yields (31-85%) with readily prepared N-Ms arylamines and commercially available 2-bromobenzyl bromide derivatives as starting materials. The potential application of the protocol was also demonstrated by the expeditious synthesis of the natural alkaloid trisphaeridine. © 2015 American Chemical Society.
        Number of references:        83
        Main heading:         Catalysis
        Controlled terms:         Chemical activation
        Uncontrolled terms:         Aryl amines - Cascade reactions - Expeditious synthesis - Nucleophilic substitutions - Palladium-catalyzed
        Classification code:         802.2 Chemical Reactions
        DOI:        10.1021/acs.joc.5b02145
        Database:        Compendex
                Compilation and indexing terms, © 2016 Elsevier Inc.
ÍøÅÌÏÂÔØ·½·¨£ºhttp://muchong.com/bbs/viewthread.php?tid=7189506Õ¾ÄÚÐÅ£ºhttp:///muchong.com/bbs/box.php
3Â¥2016-03-05 15:41:49
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû
²é¿´È«²¿ 3 ¸ö»Ø´ð

°¢´ô´ô´ô

Ìú¸Ëľ³æ (ÖªÃû×÷¼Ò)

‡å‡å³æ

¡¾´ð°¸¡¿Ó¦Öú»ØÌû

¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
Palladium-Catalyzed Nucleophilic Substitution/C-H Activation/Aromatization Cascade Reaction: One Approach To Construct 6-Unsubstituted Phenanthridines
×÷Õß:Han, WY (Han, Wenyong)[ 1 ] ; Zhou, XJ (Zhou, Xiaojian)[ 1 ] ; Yang, SY (Yang, Siyi)[ 1 ] ; Xiang, GY (Xiang, Guangyan)[ 1 ] ; Cui, BD (Cui, Baodong)[ 1 ] ; Chen, YZ (Chen, Yongzheng)[ 1 ]
JOURNAL OF ORGANIC CHEMISTRY
¾í: 80  ÆÚ: 22  Ò³: 11580-11587
DOI: 10.1021/acs.joc.5b02145
³ö°æÄê: NOV 20 2015
²é¿´ÆÚ¿¯ÐÅÏ¢
ÕªÒª
A facile and practical palladium-catalyzed nucleophilic substitution/CH activation/aromatization cascade reaction has been developed. A range of 6-unsubstituted phenanthridines could be obtained in moderate to good yields (3185%) with readily prepared N-Ms arylamines and commercially available 2-bromobenzyl bromide derivatives as starting materials. The potential application of the protocol was also demonstrated by the expeditious synthesis of the natural alkaloid trisphaeridine.
¹Ø¼ü´Ê
KeyWords PlusOLYCYCLIC AROMATIC-HYDROCARBONS; INTRAMOLECULAR DIRECT ARYLATION; TRANSITION-METAL-FREE; ONE-POT SYNTHESIS; EFFICIENT SYNTHESIS; NITROGEN-HETEROCYCLES; FUSED PHENANTHRIDINES; EXPEDITIOUS SYNTHESIS; COUPLING REACTION; CYCLIZATION
×÷ÕßÐÅÏ¢
ͨѶ×÷ÕßµØÖ·: Han, WY (ͨѶ×÷Õß)
              Zunyi Med Univ, Sch Pharm, Zunyi 563000, Peoples R China.
µØÖ·:
              [ 1 ] Zunyi Med Univ, Sch Pharm, Zunyi 563000, Peoples R China
µç×ÓÓʼþµØÖ·:hanwy@zmc.edu.cn; yzchen@zmc.edu.cn
»ù½ð×ÊÖúÖÂл
»ù½ð×ÊÖú»ú¹¹        ÊÚȨºÅ
Science and Technology Department of Guizhou Province        
2015GZ18284
QKHRCTD-2014-4002
Education Department of Guizhou Province        
QJHRCTDZ-2012-03
New Century Excellent Talent of the Ministry of Education        
NCET-13-1069
²é¿´»ù½ð×ÊÖúÐÅÏ¢   
³ö°æÉÌ
AMER CHEMICAL SOC, 1155 16TH ST, NW, WASHINGTON, DC 20036 USA
Àà±ð / ·ÖÀà
Ñо¿·½Ïò:Chemistry
Web of Science Àà±ð:Chemistry, Organic
ÎÄÏ×ÐÅÏ¢
ÎÄÏ×ÀàÐÍ:Article
ÓïÖÖ:English
Èë²ØºÅ: WOS:000365462600040
PubMed ID: 26513449
ISSN: 0022-3263
ÆÚ¿¯ÐÅÏ¢
Impact Factor (Ó°ÏìÒò×Ó): Journal Citation Reports®
ÆäËûÐÅÏ¢
IDS ºÅ: CX1NJ
Web of Science ºËÐĺϼ¯ÖÐµÄ "ÒýÓõIJο¼ÎÄÏ×": 83
Web of Science ºËÐĺϼ¯ÖÐµÄ "±»ÒýƵ´Î": 0
ÍøÅÌÏÂÔØ·½·¨£ºhttp://muchong.com/bbs/viewthread.php?tid=7189506Õ¾ÄÚÐÅ£ºhttp:///muchong.com/bbs/box.php
2Â¥2016-03-05 15:41:39
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû
×î¾ßÈËÆøÈÈÌûÍÆ¼ö [²é¿´È«²¿] ×÷Õß »Ø/¿´ ×îºó·¢±í
[¿¼ÑÐ] µ÷¼Á +10 ÔÂ@163.com 2026-04-11 10/500 2026-04-12 09:14 by zhouyuwinner
[¿¼ÑÐ] »¯¹¤µ÷¼ÁÇóµ¼Ê¦ÊÕÁô£¡Ò»Ö¾Ô¸Ê§Àû£¬Ì¤Êµ¿Ï¸É£¬ÓÐÖ²ÎïÌáÈ¡¿ÆÑо­Àú +20 yzyzx 2026-04-09 21/1050 2026-04-12 00:12 by ССССÀ²À²À²
[¿¼ÑÐ] 331Çóµ÷¼Á +5 Íõ¹ú˧ 2026-04-11 5/250 2026-04-11 22:56 by Ϫ½§Á÷Ë®
[¿¼ÑÐ] Çóµ÷¼Á +6 СÄô°®Ñ§Ï° 2026-04-11 9/450 2026-04-11 21:20 by À¶ÔÆË¼Óê
[¿¼ÑÐ] 085600²ÄÁÏÓ뻯¹¤329·ÖÇóµ÷¼Á +16 Ò¶zilin 2026-04-10 16/800 2026-04-11 11:04 by may_ÐÂÓî
[¿¼ÑÐ] ¹ã¶«Ê¡ 085601 329·ÖÇóµ÷¼Á +14 Eddieddd 2026-04-10 14/700 2026-04-11 09:58 by bljnqdcc
[²ÄÁϹ¤³Ì] ²ÄÁϵ÷¼ÁÍÆ¼ö +8 µ°¸âx2 2026-04-07 8/400 2026-04-10 23:13 by Ftglcn90
[¿¼ÑÐ] ÉúÎïѧ308·ÖÇóµ÷¼Á£¨Ò»Ö¾Ô¸»ª¶«Ê¦´ó£©×ö¹ý·Ö×ÓʵÑé +8 ÏàÐűػá¹ââÍòÕ 2026-04-07 9/450 2026-04-10 21:03 by zhouxiaoyu
[¿¼ÑÐ] ²ÄÁÏרҵ344Çóµ÷¼Á +16 hualkop 2026-04-10 21/1050 2026-04-10 17:28 by laoshidan
[¿¼ÑÐ] 314Çóµ÷¼Á +23 wakeluofu 2026-04-09 24/1200 2026-04-10 15:31 by MOF_Catal
[¿¼ÑÐ] 08600ÉúÎïÓëÒ½Ò©-327 +10 18755400796 2026-04-05 10/500 2026-04-10 08:14 by kangsm
[¿¼ÑÐ] 085600²ÄÁÏÓ뻯¹¤×¨Ë¶329 Çóµ÷¼Á +24 ¶îcc 2026-04-06 25/1250 2026-04-09 16:01 by wp06
[¿¼ÑÐ] 085801 ×Ü·Ö275 ±¾¿ÆÐÂÄÜÔ´ Çóµ÷¼Á +8 bradoner 2026-04-08 9/450 2026-04-09 13:43 by onlyÖÜ
[¿¼ÑÐ] Çóµ÷¼Á +13 Æâluck 2026-04-07 13/650 2026-04-08 22:46 by Öí»á·É
[¿¼ÑÐ] 293·ÖÇóµ÷¼Á£¬ÍâÓïΪ¶íÓï +7 ¼ÓÒ»Ò»¾Å 2026-04-07 10/500 2026-04-08 20:14 by yutian743
[¿¼ÑÐ] Ò»Ö¾Ô¸Äϲý´óѧ£¬085600£¬344·ÖÇóµ÷¼Á +11 µ÷¼ÁÉϰ¶«^ 2026-04-05 12/600 2026-04-08 16:17 by luoyongfeng
[¿¼ÑÐ] 304Çóµ÷¼Á +16 c297914 2026-04-05 17/850 2026-04-08 13:00 by grayjzr
[¿¼ÑÐ] 316Çóµ÷¼Á +7 yyxÏëµ÷¼Á 2026-04-05 7/350 2026-04-07 14:31 by shdgaomin
[¿¼ÑÐ] ÐŹ¤Ëù11408 340·Ö ±¾¿ÆÎ÷°²½»´ó×Ô¶¯»¯ +3 moontrek 2026-04-06 3/150 2026-04-07 09:56 by chongya
[¿¼ÑÐ] 312Çóµ÷¼Á +4 LR6 2026-04-06 4/200 2026-04-07 08:42 by jp9609
ÐÅÏ¢Ìáʾ
ÇëÌî´¦ÀíÒâ¼û