Heterocycles Database
Total Synthesis of
Heterocyclic
Natural Products
 
 1975-2015
 19,943 Compounds
 27 April, 2012
 
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Journal
Year
 
 Nomenclature :
 
The natural products are listed under the name used in the original literature.
 
 Journals :
 
This database lists the natural products with heterocyclic ring system whose synthesis has been determined since 1975.
The journals which have been covered are as follows.
 
Angew. Chem. Int. Ed. Engl.
Angew. Chem. Int. Ed.
Bull. Chem. Soc. Japan
Chem. and Ind.
Chem. Ber.
J. Chem. Soc., Chem. Commun.
Chem. Commun.
Chem. Eur. J.
Chemistry Lett.
Chem. Pharm. Bull.
Coll. Czech. Chem. Commun.
Eur. J. Inorg. Chem.
Eur. J. Org. Chem.
Experientia
Helv. Chim. Acta
Heterocycles
J. Am. Chem. Soc.
J. Antibiot.
J. Chem. Soc., Perkin Trans. 1
J. Heterocycl. Chem.
J. Med. Chem.
J. Nat. Prod.
J. Org. Chem.
J. Pharm. Sci.
Liebigs Ann. Chem.
Monatsh. Chem.
Org. Lett.
Phytochemistry
Planta medica
Synlett
Synth. Commun.
Synthesis
Tetrahedron
Tetrahedron Asymmetry
Tetrahedron Lett.
Yakugaku Zasshi
 
 Editor :
 
Editor
Keiichiro Fukumoto

Associate Editor
Kunio Ogasawara
Yoshiharu Iwabuchi

Assistant Editors
Naoki Kanoh
Muneo Kawasumi
Takashi Moriya
Keiichi Murakami
Kohei Sakanishi
Yusuke Sasano
Takuro Shibuta
Masatoshi Shibuya

Editorial Assistants
Sayaka Kametani
Kishiko Nakano
Yuki Shima
Kazuko Todoroki
Michi Yamamoto
 New Total Synthesis of Heterocyclic Natural Products
This journal will list natural products with heterocyclic ring system whose total synthesis has been reported.
 
27 April, 2012
Search by Group:
Polyketides
Aromatics
Terpenes
Steroids
Alkaloids
Antibiotics
Miscellaneous
 
All
 
Search by Journal :
Vol.
No.
Angew. Chem. Int. Ed.
50
37-40
Chem. Commun.
47
35, 36
Eur. J. Org. Chem.
2011
25, 26
J. Nat. Prod.
74
9
J. Org. Chem.
76
17
Org. Bio. Chem.
9
18
Org. Lett.
13
17, 18
Synlett
2011
14, 15
Synthesis
2011
17, 18
Tetrahedron
67
35, 36, 38, 39
Tetrahedron Lett.
52
36-38
  72 data found. 1 - 30 listed Next Last   

Polyketides
Ethisolide
C9H10O4 = 182
Synth. Commun.    2014, 44 , 1771
G. V. M. Sharma, D. H. Chary
DOI: 10.1080/00397911.2013.871562
CrossRef
 
chiral
racemic
Notes: formal synthesis


Polyketides
Cephalosporolide E
C10H14O4 = 198
Tetrahedron    2014, 70 , 3653
C. N. Kona, C. V. Ramana
DOI: 10.1016/j.tet.2014.04.026
CrossRef
 
chiral
racemic
Notes:


Polyketides
Cephalosporolide F
C10H14O4 = 198
Tetrahedron    2014, 70 , 3653
C. N. Kona, C. V. Ramana
DOI: 10.1016/j.tet.2014.04.026
CrossRef
 
chiral
racemic
Notes:


Polyketides
Decarestrictine I
C10H14O4 = 198
Helv. Chim. Acta    2014, 97 , 830
J. S. Yadav, M. Venkatesh, A. S. Kumar, P. A. N. Reddy, B. V. S. Reddy, A. R. Prasad
DOI: 10.1002/hlca.201300256
CrossRef
 
chiral
racemic
Notes:


Polyketides
Goniodiol, 7-epi-
C13H14O4 = 234
Synlett    2014, 25 , 1283
B. Veena, G. V. M. Sharma
DOI: 10.1055/s-0033-1341107
CrossRef
 
chiral
racemic
Notes:


Polyketides
Dihydrosporothriolide
C13H20O4 = 240
J. Org. Chem.    2014, 79 , 5908
J. Ishihara, H. Tsuru, S. Hatakeyama
DOI: 10.1021/jo5008948
CrossRef
 
chiral
racemic
Notes:


Polyketides
Avenaciolide. Iso-
C15H22O4 = 266
Synth. Commun.    2014, 44 , 1771
G. V. M. Sharma, D. H. Chary
DOI: 10.1080/00397911.2013.871562
CrossRef
 
chiral
racemic
Notes: formal synthesis


Polyketides
Cytospolide P
C17H28O6 = 328
Org. Biomol. Chem.    2014, 12 , 3358
P. Suman, B. C. Raju
DOI: 10.1039/c4ob00323c
CrossRef
 
chiral
racemic
Notes:


Polyketides
Polyrhacitide B
C20H36O6 = 372
Synthesis    2014, 46 , 1639
D. K. Mohapatra, P. S. Krishnarao, E. Bhimireddy, J. S. Yadav
DOI: 10.1055/s-0033-1341154
CrossRef
 
chiral
racemic
Notes:


Polyketides
Epiplakinic Acid F
C23H38O4 = 378
Org. Biomol. Chem.    2014, 12 , 3686
X.-Y. Tian, J.-W. Han, Q. Zhao, H. N. C. Wong
DOI: 10.1039/c4ob00448e
CrossRef
 
chiral
racemic
Notes:


Polyketides
Epiplakinic Acid F Methyl Ester
C24H40O4 = 392
Org. Biomol. Chem.    2014, 12 , 3686
X.-Y. Tian, J.-W. Han, Q. Zhao, H. N. C. Wong
DOI: 10.1039/c4ob00448e
CrossRef
 
chiral
racemic
Notes:


Polyketides
Bitungolide E
C25H34O4 = 398
Org. Biomol. Chem.    2014, 12 , 4002
K. M. Reddy, J. Shashidhar, S. Ghosh
DOI: 10.1039/c4ob00250d
CrossRef
 
chiral
racemic
Notes:


Polyketides
Plakortone L
C26H40O3 = 400
Org. Lett.    2014, 16 , 3384
H. Sugimura, S. Sato, K. Tokudome, T. Yamada
DOI: 10.1021/ol501446w
CrossRef
 
chiral
racemic
Notes:


Polyketides
Biselyngbyolide A
C27H42O5 = 446
Org. Lett.    2014, 16 , 2858
Y. Tanabe, E. Sato, N. Nakajima, A. Ohkubo, O. Ohno, K. Suenaga
DOI: 10.1021/ol500996n
CrossRef
 
chiral
racemic
Notes:


Polyketides
Bitungolide B
C25H33O5Cl = 448.5
Org. Biomol. Chem.    2014, 12 , 4002
K. M. Reddy, J. Shashidhar, S. Ghosh
DOI: 10.1039/c4ob00250d
CrossRef
 
chiral
racemic
Notes:


Polyketides
GEX1Q1
C25H42O7 = 454
Org. Lett.    2014, 16 , 3154
A. K. Ghosh, N. Ma, K. A. Effenberger, M. S. Jurica
DOI: 10.1021/ol501345d
CrossRef
 
chiral
racemic
Notes:


Polyketides
Sekothrixide
C28H50O6 = 482
Org. Lett.    2014, 16 , 2794
N. Terayama, E. Yasui, M. Mizukami, M. Miyashita, S. Nagumo
DOI: 10.1021/ol5006856
CrossRef
 
chiral
racemic
Notes: revised structure


Polyketides
FR901464
C27H41NO8 = 507
J. Org. Chem.    2014, 79 , 5697
A. K. Ghosh, Z.-H. Chen, K. A. Effenberger, M. S. Jurica
DOI: 10.1021/jo500800k
CrossRef
 
chiral
racemic
Notes:


Polyketides
Spliceostatin A
C28H43NO8 = 521
J. Org. Chem.    2014, 79 , 5697
A. K. Ghosh, Z.-H. Chen, K. A. Effenberger, M. S. Jurica
DOI: 10.1021/jo500800k
CrossRef
 
chiral
racemic
Notes:


Aromatics
Xylarinol B
C13H18O3 = 222
Chem. Asian J.    2014, 9 , 1557
A. A. More, C. V. Ramana
DOI: 10.1002/asia.201301647
CrossRef
 
chiral
racemic
Notes: proposed structure


Aromatics
No Name
C14H15NO3 = 245
Org. Biomol. Chem.    2014, 12 , 4098
K. Kashinath, P. D. Jadhav, D. S. Reddy
DOI: 10.1039/c4ob00300d
CrossRef
 
chiral
racemic
Notes: synthesis of enantiomer


Aromatics
Dugesin B
C20H14O5 = 334
Org. Lett.    2014, 16 , 3376
C. Fu, Y. Zhang, J. Xuan, C. Zhu, B. Wang, H. Ding
DOI: 10.1021/ol501423t
CrossRef
 
chiral
racemic
Notes:


Aromatics
Salvileucalin C
C20H14O5 = 334
Org. Lett.    2014, 16 , 3376
C. Fu, Y. Zhang, J. Xuan, C. Zhu, B. Wang, H. Ding
DOI: 10.1021/ol501423t
CrossRef
 
chiral
racemic
Notes:


Aromatics
Salvileucalin D
C20H14O5 = 334
Org. Lett.    2014, 16 , 3376
C. Fu, Y. Zhang, J. Xuan, C. Zhu, B. Wang, H. Ding
DOI: 10.1021/ol501423t
CrossRef
 
chiral
racemic
Notes:


Aromatics
Salvipuberulin
C20H14O5 = 334
Org. Lett.    2014, 16 , 3376
C. Fu, Y. Zhang, J. Xuan, C. Zhu, B. Wang, H. Ding
DOI: 10.1021/ol501423t
CrossRef
 
chiral
racemic
Notes:


Aromatics
Salvipuberulin, Iso-
C20H14O5 = 334
Org. Lett.    2014, 16 , 3376
C. Fu, Y. Zhang, J. Xuan, C. Zhu, B. Wang, H. Ding
DOI: 10.1021/ol501423t
CrossRef
 
chiral
racemic
Notes:


Aromatics
Liphagal
C22H28O4 = 356
Eur. J. Org. Chem.    2014, 2014 , 3443
T. Kamishima, T. Kikuchi, K. Narita, T. Katoh
DOI: 10.1002/ejoc.201402082
CrossRef
 
chiral
racemic
Notes:


Aromatics
Virgatolide B
C19H24O7 = 364
J. Org. Chem.    2014, 79 , 5269
P. A. Hume, D. P. Furkert, M. A. Brimble
DOI: 10.1021/jo5008527
CrossRef
 
chiral
racemic
Notes:


Aromatics
α-Tocopherol
C29H50O2 = 430
Eur. J. Org. Chem.    2014, 2014 , 3337
A. O. Termath, J. Velder, R. T. Stemmler, T. Netscher, W. Bonrath, H.-G. Schmalz
DOI: 10.1002/ejoc.201402240
CrossRef
 
chiral
racemic
Notes:


Aromatics
Polycarcin V
C27H26O9 = 494
Org. Lett.    2014, 16 , 2962
X. Cai, K. Ng, H. Panesar, S.-J. Moon, M. Paredes, K. Ishida, C. Hertweck, T. G. Minehan
DOI: 10.1021/ol501095w
CrossRef
 
chiral
racemic
Notes:


  72 data found. 1 - 30 listed Next Last   
   
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