±±¾©Ê¯ÓÍ»¯¹¤Ñ§Ôº2026ÄêÑо¿ÉúÕÐÉú½ÓÊÕµ÷¼Á¹«¸æ
²é¿´: 348  |  »Ø¸´: 2

chumjun

гæ (ÕýʽдÊÖ)

[ÇóÖú] CÆ×ÇóÖú»¯ºÏÎï½á¹¹ ÒÑÓÐ2È˲ÎÓë

ë®´úÈܼÁ£ºDMSO
CÆ×Êý¾Ý£º14.4,20.0,22.6,23.6,26.8,29.0,29.2,29.3,29.4,29.7,30.1,30.3,31.6,31.7,32.5,34.7,34.9,36.8,43.2,118.9,124.6,124.7,138.3,138.4,147.4,147.5,147.6,209
»Ø¸´´ËÂ¥

» ²ÂÄãϲ»¶

» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:

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

yangyinhe

ÖÁ×ðľ³æ (ÖøÃûдÊÖ)

¡¾´ð°¸¡¿Ó¦Öú»ØÌû

¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
1 .     5,13-Dimethyl-1,5-heptadecadiene
    ÏàËÆ¶È:65.5%
Bioscience, Biotechnology, and Biochemistry          2009          73          1618-1622
Synthesis and Field Evaluation of Methyl-branched Ketones, Sex Pheromone Components Produced by Lithosiinae Female Moths in the Family of Arctiidae
Nguyen Duc DO, Masakatsu KINJO, Tomonori TAGURI, Yasushi ADACHI, Rei YAMAKAWA and Tetsu ANDO
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

2 .     2¦Â-(diundecylamino)-5¦Á-androstane-3¦Á,17¦Â-diol
C41H77NO2     ÏàËÆ¶È:65.5%
Bioorganic & Medicinal Chemistry          2008          16          5062-5077
Chemical synthesis of 2¦Â-amino-5¦Á-androstane-3¦Á,17¦Â-diol N-derivatives and their antiproliferative effect on HL-60 human leukemia cells
Dominic Thibeault, Jenny Roy, Patrick DeRoy, Donald Poirier
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

3 .     3-decyl-5,7-dimethyl-2-undecylquinoline
C32H53N     ÏàËÆ¶È:64.2%
Journal of Heterocyclic Chemistry          2004          41          423-429
Ruthenium-catalyzed formal alkyl group transfer: Synthesis of quinolines from nitroarenes and alkylammonium halides
Chan Sik Cho,Na Young Lee,Tae-Jeong Kim and Sang Chul Shim
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

4 .     2¦Â-(dinonylamino)-5¦Á-androstane-3¦Á,17¦Â-diol
C37H69NO2     ÏàËÆ¶È:60.7%
Bioorganic & Medicinal Chemistry          2008          16          5062-5077
Chemical synthesis of 2¦Â-amino-5¦Á-androstane-3¦Á,17¦Â-diol N-derivatives and their antiproliferative effect on HL-60 human leukemia cells
Dominic Thibeault, Jenny Roy, Patrick DeRoy, Donald Poirier
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

5 .     2-(hexadecylsulfanyl)-3-(pentylsulfanyl)-1,4-naphthoquinone
C31H48O2S2     ÏàËÆ¶È:60.7%
Russian Journal of Organic Chemistry          2010          46          209-215
Synthesis and spectral properties of 1,4-naphthoquinone sulfanyl derivatives
C. Sayil and C. Ibis
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

6 .     2-(butylsulfanyl)-3-(hexadecylsulfanyl)-1,4-naphthoquinone
C30H46O2S2     ÏàËÆ¶È:60.7%
Russian Journal of Organic Chemistry          2010          46          209-215
Synthesis and spectral properties of 1,4-naphthoquinone sulfanyl derivatives
C. Sayil and C. Ibis
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

7 .     compound 18
C112H164O4N4     ÏàËÆ¶È:60.7%
European Journal of Organic Chemistry          2011                   3016-3025
C4-Symmetric Alkoxyresorcin[4]arene Triflates: The Use of Palladium-Catalyzed Reactions in the Synthesis of Axially Chiral Derivatives with Amino- and/or Alkoxy-Substituents
Philip C. Bulman Page, Terence R. Bygrave, Yohan Chan, Harry Heaney and Vickie McKee
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

8 .     compound 20
C100H164O4N4     ÏàËÆ¶È:60.7%
European Journal of Organic Chemistry          2011                   3016-3025
C4-Symmetric Alkoxyresorcin[4]arene Triflates: The Use of Palladium-Catalyzed Reactions in the Synthesis of Axially Chiral Derivatives with Amino- and/or Alkoxy-Substituents
Philip C. Bulman Page, Terence R. Bygrave, Yohan Chan, Harry Heaney and Vickie McKee
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

9 .     (2S,3S)-2-(13-Bromotridecyl)-3-((R)-1-methylheptadecyl)oxirane
C33H65BrO     ÏàËÆ¶È:60.7%
Tetrahedron          2014          70          7322-7335
Synthetic epoxy-mycolic acids
Dakhil Z. Al Kremawi, Juma'a R. Al Dulayymi, Mark S. Baird
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

10 .     Bullatacinone
    ÏàËÆ¶È:60%
Journal of Natural Products          1989          Vol 52          463
Bullatacin and Bullatacinone: Two Highly Potent Bioactive Acetogenins from Annona bullata
Y.-H. Hui, J. K. Rupprecht, Y. M. Liu, J. E. Anderson, D. L. Smith, C.-J. Chang, J. L. McLaughlin
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2Â¥2015-01-28 16:08:06
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû

lifeliuyan

ÖÁ×ðľ³æ (Ö°Òµ×÷¼Ò)

¡¾´ð°¸¡¿Ó¦Öú»ØÌû

¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
chumjun: ½ð±Ò+10, ¡ïÓаïÖú 2015-01-29 09:43:47
²éѯ½á¹û£º¹²²éµ½601¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)
1 .     5,13-Dimethyl-1,5-heptadecadiene
    ÏàËÆ¶È:65.5%
Bioscience, Biotechnology, and Biochemistry          2009          73          1618-1622
Synthesis and Field Evaluation of Methyl-branched Ketones, Sex Pheromone Components Produced by Lithosiinae Female Moths in the Family of Arctiidae
Nguyen Duc DO, Masakatsu KINJO, Tomonori TAGURI, Yasushi ADACHI, Rei YAMAKAWA and Tetsu ANDO
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2 .     2¦Â-(diundecylamino)-5¦Á-androstane-3¦Á,17¦Â-diol
C41H77NO2     ÏàËÆ¶È:65.5%
Bioorganic & Medicinal Chemistry          2008          16          5062-5077
Chemical synthesis of 2¦Â-amino-5¦Á-androstane-3¦Á,17¦Â-diol N-derivatives and their antiproliferative effect on HL-60 human leukemia cells
Dominic Thibeault, Jenny Roy, Patrick DeRoy, Donald Poirier
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
3 .     3-decyl-5,7-dimethyl-2-undecylquinoline
C32H53N     ÏàËÆ¶È:64.2%
Journal of Heterocyclic Chemistry          2004          41          423-429
Ruthenium-catalyzed formal alkyl group transfer: Synthesis of quinolines from nitroarenes and alkylammonium halides
Chan Sik Cho,Na Young Lee,Tae-Jeong Kim and Sang Chul Shim
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
4 .     2¦Â-(dinonylamino)-5¦Á-androstane-3¦Á,17¦Â-diol
C37H69NO2     ÏàËÆ¶È:60.7%
Bioorganic & Medicinal Chemistry          2008          16          5062-5077
Chemical synthesis of 2¦Â-amino-5¦Á-androstane-3¦Á,17¦Â-diol N-derivatives and their antiproliferative effect on HL-60 human leukemia cells
Dominic Thibeault, Jenny Roy, Patrick DeRoy, Donald Poirier
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
5 .     2-(hexadecylsulfanyl)-3-(pentylsulfanyl)-1,4-naphthoquinone
C31H48O2S2     ÏàËÆ¶È:60.7%
Russian Journal of Organic Chemistry          2010          46          209-215
Synthesis and spectral properties of 1,4-naphthoquinone sulfanyl derivatives
C. Sayil and C. Ibis
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
6 .     2-(butylsulfanyl)-3-(hexadecylsulfanyl)-1,4-naphthoquinone
C30H46O2S2     ÏàËÆ¶È:60.7%
Russian Journal of Organic Chemistry          2010          46          209-215
Synthesis and spectral properties of 1,4-naphthoquinone sulfanyl derivatives
C. Sayil and C. Ibis
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
7 .     compound 18
C112H164O4N4     ÏàËÆ¶È:60.7%
European Journal of Organic Chemistry          2011                   3016-3025
C4-Symmetric Alkoxyresorcin[4]arene Triflates: The Use of Palladium-Catalyzed Reactions in the Synthesis of Axially Chiral Derivatives with Amino- and/or Alkoxy-Substituents
Philip C. Bulman Page, Terence R. Bygrave, Yohan Chan, Harry Heaney and Vickie McKee
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
8 .     compound 20
C100H164O4N4     ÏàËÆ¶È:60.7%
European Journal of Organic Chemistry          2011                   3016-3025
C4-Symmetric Alkoxyresorcin[4]arene Triflates: The Use of Palladium-Catalyzed Reactions in the Synthesis of Axially Chiral Derivatives with Amino- and/or Alkoxy-Substituents
Philip C. Bulman Page, Terence R. Bygrave, Yohan Chan, Harry Heaney and Vickie McKee
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
9 .     (2S,3S)-2-(13-Bromotridecyl)-3-((R)-1-methylheptadecyl)oxirane
C33H65BrO     ÏàËÆ¶È:60.7%
Tetrahedron          2014          70          7322-7335
Synthetic epoxy-mycolic acids
Dakhil Z. Al Kremawi, Juma'a R. Al Dulayymi, Mark S. Baird
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
10 .     Bullatacinone
    ÏàËÆ¶È:60%
Journal of Natural Products          1989          Vol 52          463
Bullatacin and Bullatacinone: Two Highly Potent Bioactive Acetogenins from Annona bullata
Y.-H. Hui, J. K. Rupprecht, Y. M. Liu, J. E. Anderson, D. L. Smith, C.-J. Chang, J. L. McLaughlin
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
11 .     9-((1R,2R)-2-((2S,19S,20S)-19-methoxy-20-methyloctatriacontan-2-yl)cyclopropyl)nonanal
C52H102O2     ÏàËÆ¶È:60%
Tetrahedron          2013          69          6285-6296
The synthesis of methoxy and keto mycolic acids containing methyl-trans-cyclopropanes
Gani Koza, Maged Muzael, Richard R. Schubert-Rowles, Cornelia Theunissen, Juma'a R. Al Dulayymi, Mark S. Baird
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
12 .     abiet¦Á-8,11,13-trien-18-yl hexadecanoate
C36H60O2     ÏàËÆ¶È:59.3%
Phytochemistry          2008          69          498-505
Diterpene constituents of leaves from Juniperus brevifolia
Ana M.L. Seca, Artur M.S. Silva, Isabel L. Bazzocchi, Ignacio A. Jimenez
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
13 .     5,13-Dimethyl-5-heptadecen-1-ol
    ÏàËÆ¶È:58.6%
Bioscience, Biotechnology, and Biochemistry          2009          73          1618-1622
Synthesis and Field Evaluation of Methyl-branched Ketones, Sex Pheromone Components Produced by Lithosiinae Female Moths in the Family of Arctiidae
Nguyen Duc DO, Masakatsu KINJO, Tomonori TAGURI, Yasushi ADACHI, Rei YAMAKAWA and Tetsu ANDO
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
14 .     palmitate
C36H70O2     ÏàËÆ¶È:58.6%
Natural Product Communications          2011          6          767-772
Lipophilic Components from the Ecuadorian Plant Schistocarpha eupatorioides
Gianluca Gilardoni, Solveig Tosi, Giorgio Mellerio, Maria Elena Maldonado, Ximena Chiriboga and Giovanni Vidari
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
15 .     2¦Â-(n-dodecylamino)-5¦Á-androstane-3¦Á,17¦Â-diol
C31H57NO2     ÏàËÆ¶È:58.0%
Bioorganic & Medicinal Chemistry          2008          16          5062-5077
Chemical synthesis of 2¦Â-amino-5¦Á-androstane-3¦Á,17¦Â-diol N-derivatives and their antiproliferative effect on HL-60 human leukemia cells
Dominic Thibeault, Jenny Roy, Patrick DeRoy, Donald Poirier
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
16 .     6-decyl-2-hydroxyazulene
C20H28O     ÏàËÆ¶È:58.0%
Tetrahedron          2013          69          4259-4269
Efficient synthesis and redox behavior of a series of 6-alkyl-2-phenylazulenes
Shunji Ito, Mao Ueda, Ryuta Sekiguchi, Jun Kawakami
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
17 .     (2¦Â,4a¦Â)-1-{2-(8-amino-2,3,4,4a-tetrahydro-6-nonylpyrimido[3,4-b][1,2]oxazinyl)}-2-undecanone
C27H49N3O2     ÏàËÆ¶È:57.1%
Journal of Natural Products          1999          62          1707-1711
Revision of the Stereochemistry of Batzelladine F. Approaches to the Tricyclic Hydroxyguanidine Moiety of Batzelladines G, H, and I
Barry B. Snider and Marina V. Busuyek
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
18 .     Termitomycamide C
C28H44N2O3     ÏàËÆ¶È:57.1%
Organic Letters          2010          Vol.12,No.21          5012-5015
Termitomycamides A to E, Fatty Acid Amides Isolated from the Mushroom Termitomyces titanicus, Suppress Endoplasmic Reticulum Stress
Jae-Hoon Choi,Kohei Maeda,Kaoru Nagai, Etsuko Harada, Mitsuo Kawade,Hirofumi Hirai, and Hirokazu Kawagishi
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
19 .     brachystine
C23H41NO     ÏàËÆ¶È:57.1%
Phytochemistry          1988          27          3523-3527
Minor amides of Piper species
S.K. Koul,S.C. Taneja,V.K. Agarwal,K.L. Dhar
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
20 .     2,3,4,5-Tetra(5-dodecylthiophen-2-yl)thiophene
C68H108S5     ÏàËÆ¶È:57.1%
Tetrahedron          2012          68          1192-1197
Synthesis and characterization of new planar butterfly-shaped fused oligothiophenes
Jing Wang, Huan Xu, Bin Li, Xiao-Ping Cao, Hao-Li Zhang
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
3Â¥2015-01-28 16:09:24
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû
Ïà¹Ø°æ¿éÌø×ª ÎÒÒª¶©ÔÄÂ¥Ö÷ chumjun µÄÖ÷Ìâ¸üÐÂ
×î¾ßÈËÆøÈÈÌûÍÆ¼ö [²é¿´È«²¿] ×÷Õß »Ø/¿´ ×îºó·¢±í
[¿¼ÑÐ] ²ÄÁϵ÷¼Á +8 ¸ï΢¹ð 2026-04-04 8/400 2026-04-04 23:36 by lqwchd
[¿¼ÑÐ] 294Çóµ÷¼Á +6 Grey_Ey 2026-04-02 9/450 2026-04-04 22:07 by hemengdong
[¿¼ÑÐ] 277Çóµ÷¼Á +4 12A3 2026-04-02 5/250 2026-04-04 20:28 by À¶ÔÆË¼Óê
[¿¼ÑÐ] 342Çóµ÷¼Á +3 Liang7111 2026-04-04 5/250 2026-04-04 19:47 by dongzh2009
[¿¼ÑÐ] 306Çóµ÷¼Á +3 hybÉÏÃû¹¤ 2026-04-02 3/150 2026-04-04 18:12 by ÈÈÇéɳĮ
[¿¼ÑÐ] ²ÄÁÏ¿ÆÑ§Ó빤³Ì¿¼ÑÐ +10 Õü¾ÈÆ¤ÌØÍÐÏÈÉú 2026-04-02 10/500 2026-04-03 23:57 by userper
[¿¼ÑÐ] 350Ò»Ö¾Ô¸±±¾©º½¿Õº½Ìì´óѧ08500²ÄÁÏ¿ÆÑ§Ó빤³ÌÇóµ÷¼Á +5 kjnasfss 2026-04-03 5/250 2026-04-03 22:29 by Î޼ʵIJÝÔ­
[¿¼ÑÐ] 372·Ö²ÄÁÏÓ뻯¹¤£¨085600£©Ò»Ö¾Ô¸ºþÄÏ´óѧÇóµ÷¼Á +3 À¶¼ãƬ 2026-04-03 4/200 2026-04-03 17:58 by Jimmyandyou
[¿¼ÑÐ] ÉúÎïѧ308·ÖÇóµ÷¼Á£¨Ò»Ö¾Ô¸»ª¶«Ê¦´ó£© +7 ÏàÐűػá¹ââÍòÕ 2026-04-02 7/350 2026-04-03 16:48 by rzh123456
[¿¼ÑÐ] Ò»Ö¾Ô¸ÉúÎïÓëÒ½Ò©£¬296·Ö£¬Çóµ÷¼Á +8 66¹ 2026-04-03 9/450 2026-04-03 14:22 by »¯Ñ§»¯¹¤Ë¶Ê¿ÕÐÉ
[¿¼ÑÐ] 311Çóµ÷¼ÁÒ»Ö¾Ô¸ºÏ·Ê¹¤Òµ´óѧ +15 Çï¶þÊ®¶þ 2026-03-30 15/750 2026-04-03 10:19 by linyelide
[¿¼ÑÐ] ũѧ¿¼ÑÐÇóµ÷¼Á +3 dkdkxm 2026-04-01 3/150 2026-04-02 16:04 by wangjagri
[¿¼ÑÐ] 285Çóµ÷¼Á +14 AZMK 2026-04-02 14/700 2026-04-02 15:54 by ÉϾÅÌìÀ¿Ô£¨ºÃÔ
[¿¼²©] ²ÄÁϹ¤³Ìרҵ˶ʿÉ격 +3 ÷ëÕýÓî 2026-03-30 3/150 2026-04-02 15:04 by greychen00
[¿¼ÑÐ] 286·Öµ÷¼Á +20 Faune 2026-03-30 22/1100 2026-04-02 13:24 by clyblh
[¿¼ÑÐ] Ò»Ö¾Ô¸±±½»²ÄÁϹ¤³Ì×Ü·Ö358 +5 cs0106 2026-04-01 7/350 2026-04-01 11:45 by wangjy2002
[¿¼ÑÐ] »·¾³¹¤³Ì 085701£¬267Çóµ÷¼Á +15 minht 2026-03-29 16/800 2026-04-01 10:13 by li_sujuan99
[¿¼ÑÐ] 274Çóµ÷¼Á +6 xiao°®Í¬Ñ§ 2026-03-30 6/300 2026-03-31 10:04 by cal0306
[¿¼ÑÐ] 285Çóµ÷¼Á +6 AZMK 2026-03-29 9/450 2026-03-30 21:02 by dophin1985
[¿¼ÑÐ] 296Çóµ÷¼Á +10 ±Ë°¶t 2026-03-29 10/500 2026-03-30 10:50 by ̽123
ÐÅÏ¢Ìáʾ
ÇëÌî´¦ÀíÒâ¼û