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1 .     methyl 2,2-dimethyl-3-N'-(4'-trifluoromethylbenzoyl)hydrazinononanoate
C20H29N2O3F3     ÏàËÆ¶È:61.1%
Heterocycles          2000          52          1143-1162
Mannich Type Reactions of Acylhydrazones with Silyl Enolates for the Synthesis of ¦Â-Amino Ester, ¦Â-Amino Ketone, ¦Â-Lactam, Pyrazolidinone, and Pyrazolone Derivatives
Osamu Okitsu, Hidekazu Oyamada, Takayuki Furuta, and Shu Kobayashi*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     (S)-2-[[hydroxy(4-phenylbutyl)phosphinyl]oxy]-6-[[(phenylmethoxy)carbonyl]amino]hexanoic acid monomethyl ester
     ÏàËÆ¶È:61.1%
Journal of Medicinal Chemistry          1990          33          1459-1469
(Phosphinyloxy)acyl amino acid inhibitors of angiotensin converting enzyme. 2. Terminal amino acid analogs of (S)-1-[6-amino-2-[[hydroxy(4-phenylbutyl)phosphinyl]oxy]-1-oxohexyl]-L-proline
Donald S. Karanewsky, Michael C. Badia, David W. Cushman, Jack M. DeForrest, Tamara Dejneka, Ving G. Lee, Melanie J. Loots, Edward W. Petrillo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     methyl 1-benzyl-7,7-dimethyl-2,5-dioxo-1,2,3,4,5,6,7,8-octahydroquinoline-3-carboxylate
C20H23NO4     ÏàËÆ¶È:61.1%
Tetrahedron          2013          69          9406-9416
Lithium perchlorate-, acetic anhydride-, and triphenylphosphine-assisted multicomponent syntheses of 4-unsubstituted 2,5-dioxooctahydroquinoline-3-carboxylates and 3-carbonitriles Original Research Article
Xingxian Gu, Gunda I. Georg
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     1,3,13-Vuiparatriene
     ÏàËÆ¶È:60%
Phytochemistry          1993          34          747-750
Diterpenes with a valparane skeleton
Julio G. Urones, Isidro S. Marcos, Pilar Basabe, Concepci¨®n Alonso, Isabel M. Oliva, Narciso M. Garrido, David D. Mart¨ªn, Anna M. Lithgow
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     4-(2-chloro-3-quinolyl)-7,7-dimethyl-5-oxo-1,2,3,4,5,6,7,8-octahydroquinazoline-2-thione
C19H18ClN3OS     ÏàËÆ¶È:57.8%
Journal of Heterocyclic Chemistry          2005          42          703-705
Microwave induced new route to acridine and quinazoline derivatives using TLC plates
M. Kidwai,S. Saxena and R. Mohan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     1-(2-Cyclohexen-1-yloxymethyl)-6-(3,5-dimethylbenzyl)-5-isopropyluracil
C23H30N2O3     ÏàËÆ¶È:57.8%
Archiv der Pharmazie          2003          336          236-241
Synthesis of Novel MKC-442 Analogues with Potent Activities against HIV-1
Nasser R. El-Brollosy, Erik B. Pedersen and Claus Nielsen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     7,8,7',8'-Tetrahydro-¦Â,¦Â-carotene
C40H60     ÏàËÆ¶È:57.8%
Journal of Natural Products          2012          75          975-979
Stereoselective Synthesis by Olefin Metathesis and Characterization of ¦Ç-Carotene (7,8,7¡ä,8¡ä-tetrahydro-¦Â,¦Â-carotene)
Noelia Font¨¢n, Rosana Alvarez, and Angel R. de Lera
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     (1R,2S)-8-[(isopropylamino)carbonyl]-1-methyl-2-(dipropylamino)tetralin hydrochloride
C21H34N2O     ÏàËÆ¶È:57.8%
Journal of Medicinal Chemistry          1995          38          150-160
Derivatives of cis-2-Amino-8-hydroxy-1-methyltetralin: Mixed 5-HT1A-Receptor Agonists and Dopamine D2-Receptor Antagonists
Ye Liu, Hong Yu, Nina Mohell, Gunnar Nordvall, Tommy Lewander, Uli Hacksell
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     4-(2-pentyl-5-phenylbenzofuran-7-yl)morpholine
C23H27NO2     ÏàËÆ¶È:57.8%
Tetrahedron          2013          69          1857-1871
Multisubstituted benzofurans through a copper- and/or palladium-catalyzed assembly and functionalization process
Antonio Arcadi, Federico Blesi, Sandro Cacchi, Giancarlo Fabrizi, Antonella Goggiamani, Fabio Marinelli
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     N¦Á-(tert-butyloxycarbonyl)-NЄ-(9-fluorenylmethoxycarbonyl)-D-lysine allyl ester
C29H36O6N2     ÏàËÆ¶È:57.1%
The Journal of Organic Chemistry          1997          62          6199-6203
Solid-Phase Total Synthesis of Oscillamide Y and Analogues
Ian R. Marsh and Mark Bradley, Simon J. Teague
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     1-hydroxycryprochine
C18H23NO3     ÏàËÆ¶È:55.5%
Chemical & Pharmaceutical Bulletin          2001          49(10)          1292-1294
Alkaloids from the Leaves of Cryptocarya chinensis HEMSL.
Fu-Wen LIN, Pei-Lin WU, and Tian-Shung WU
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     populene C
C18H20O3     ÏàËÆ¶È:55.5%
Journal of Natural Products          2008          71(7)          1173-1177
Cytotoxic and Antibacterial Sesquiterpenes from Thespesia populnea
Sompong Boonsri, Chatchanok Karalai, Chanita Ponglimanont,Suchada Chantrapromma, and Akkharawit Kanjana-opas
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     ¦Â-Costol
C15H24O     ÏàËÆ¶È:55.5%
Phytochemistry          1996          41          243-246
Two guaiane and eudesmane-type sesquiterpenoids from Neocallitropsis pancheri
Phila Raharivelomanana, Jean-Pierre Bianchini, Robert Faure, Aim¨¦ Cambon, Marcel Azzaro
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     8¦Á-angeloxyloxybicyclogermacrene
     ÏàËÆ¶È:55.5%
Phytochemistry          1992          31          203-207
Sesquiterpenes and phenylpropanoids from Seseli vayredanum
Alejandro F. Barrero, M. Mar Herrador, Pilar Arteaga
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     (6aS,12bS)-3-methyl-5,6,6a,7,8,12b-hexahydrobenzo[a]phenanthridine
C18H19N     ÏàËÆ¶È:55.5%
Organic Letters          2011          Vol.13,No.12          3000-3003
Diastereoselective Intramolecular Friedel-Crafts Alkylation of Tetralins
Cl¨¦mence Li¨¦bert, Marion K. Brinks, Andrew G. Capacci, Matthew J. Fleming, and Mark Lautens
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     1-(6,7-Dimethoxy-1-methyl-3,4-dihydroisoquinolin-2(1H)-yl)-2-phenylethanone
C20H23NO3     ÏàËÆ¶È:55.5%
Molecules          2011          16          7019-7042
Synthesis and Contractile Activity of Substituted 1, 2, 3, 4-Tetrahydroisoquinolines
Iliyan Ivanov, Stoyanka Nikolova, Dimo Aladjov, Iliyana Stefanova and Plamen Zagorchev
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     3,3,6,6-tetramethyl-9-(2-chloro-3-quinolyl)-1,2,3,4,5,6,7,8,9,10-decahydroacridine-1,8-dione
C26H27ClNO2     ÏàËÆ¶È:55.5%
Journal of Heterocyclic Chemistry          2005          42          703-705
Microwave induced new route to acridine and quinazoline derivatives using TLC plates
M. Kidwai,S. Saxena and R. Mohan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     compound 2
C20H30O4     ÏàËÆ¶È:55.5%
Indian Journal of Chemistry Section B          2007          46B          985-988
Coumarin dimer and sesquiterpene lactones from Carpesium lipskyi Winkl
Wang,Jian Nong; Gu,Shi Ping; Tan,Ren Xiang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     (1R,2S,5R)-2-isopropyl-5-methyl-1-[(2-hydroxymethylphenyl)methyl]cyclohexanol
C18H28O2     ÏàËÆ¶È:55.5%
Heterocycles          2007          74          507-519
Cyclic Acetals as Precursors of Substituted Isochromans and Naphthoxepines
Daniel Garc¨ªa, Francisco Foubelo, and Miguel Yus
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     4-[(1S,6S)-2,2,6-Trimethyl-6-(pyridin-2-ylsulfanyl)cyclohexyl]butan-2-one
C18H27NOS     ÏàËÆ¶È:55.5%
Chemistry & Biodiversity          2010          7          421-439
Bioactive Compounds with Added Value Prepared from Terpenes Contained in Solid Wastes from the Olive Oil Industry
Andres Parra, Pilar E. Lopez and Andres Garcia-Granados
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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