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
  76 data found. 1 - 30 listed Next Last   

Polyketides
Recifeiolide
C12H20O2 = 196
Tetrahedron    2014, 70 , 2944
D. M. Zubrytski, D. G. Kananovich, O. G. Kulinkovich
DOI: 10.1016/j.tet.2014.03.032
CrossRef
 
chiral
racemic
Notes:


Polyketides
Gamahonolide A
C12H20O3 = 212
Tetrahedron Lett.    2014, 55 , 3227
G. Sabitha, K. P. Reddy, S. P. Reddy, J. S. Yadav
DOI: 10.1016/j.tetlet.2014.04.026
CrossRef
 
chiral
racemic
Notes:


Polyketides
Disparlure
C19H38O = 282
Eur. J. Org. Chem.    2014, , 3249
V. Bethi, P. Kattanguru, R. A. Fernandes
DOI: 10.1002/ejoc.201400021
CrossRef
 
chiral
racemic
Notes: synthesis of both enantiomers


Polyketides
Jaspine B
C18H37NO2 = 299
Tetrahedron Asymmetry    2014, 25 , 750
M. Martinková, E. Mezeiová, J. Gonda, D. Jacková, K. Pomikalová
DOI: 10.1016/j.tetasy.2014.04.002
CrossRef
 
chiral
racemic
Notes: synthesis of the enantiomer


Polyketides
Cananginone H
C21H32O3 = 332
Tetrahedron    2014, 70 , 2905
T. K. Kuilya, S. Chatterjee, R. K. Goswami
DOI: 10.1016/j.tet.2014.03.028
CrossRef
 
chiral
racemic
Notes:


Polyketides
Cananginone I
C21H34O3 = 334
Tetrahedron    2014, 70 , 2905
T. K. Kuilya, S. Chatterjee, R. K. Goswami
DOI: 10.1016/j.tet.2014.03.028
CrossRef
 
chiral
racemic
Notes:


Polyketides
Pseudomonic Acid Methyl Monate
C18H30O6 = 342
Org. Biomol. Chem.    2014, 12 , 2950
Y. Sridhar, P. Srihari
DOI: 10.1039/c4ob00025k
CrossRef
 
chiral
racemic
Notes:


Polyketides
Synargentolide-B
C16H22O8 = 342
Tetrahedron Lett.    2014, 55 , 3087
S. Konda, K. Bhaskar, L. Nagarapu, D. M. Akkewar
DOI: 10.1016/j.tetlet.2014.03.133
CrossRef
 
chiral
racemic
Notes:


Polyketides
Synrotolide
C16H22O8 = 342
Tetrahedron Asymmetry    2014, 25 , 856
G. Sabitha, A. S. Rao, A. Sandeep, B. M. Latha, D. V. Reddy
DOI: 10.1016/j.tetasy.2014.04.010
CrossRef
 
chiral
racemic
Notes:


Polyketides
Cananginone E
C23H36O3 = 360
Tetrahedron    2014, 70 , 2905
T. K. Kuilya, S. Chatterjee, R. K. Goswami
DOI: 10.1016/j.tet.2014.03.028
CrossRef
 
chiral
racemic
Notes:


Polyketides
Cananginone F
C23H38O3 = 362
Tetrahedron    2014, 70 , 2905
T. K. Kuilya, S. Chatterjee, R. K. Goswami
DOI: 10.1016/j.tet.2014.03.028
CrossRef
 
chiral
racemic
Notes:


Polyketides
Cananginone D
C24H38O3 = 374
Tetrahedron    2014, 70 , 2905
T. K. Kuilya, S. Chatterjee, R. K. Goswami
DOI: 10.1016/j.tet.2014.03.028
CrossRef
 
chiral
racemic
Notes:


Polyketides
Cananginone G
C24H40O3 = 376
Tetrahedron    2014, 70 , 2905
T. K. Kuilya, S. Chatterjee, R. K. Goswami
DOI: 10.1016/j.tet.2014.03.028
CrossRef
 
chiral
racemic
Notes:


Polyketides
Aculeatin A
C26H42O4 = 418
Synthesis    2014, 46 , 1205
L. Maram, B. Das
DOI: 10.1055/s-0033-1340866
CrossRef
 
chiral
racemic
Notes:


Polyketides
Aculeatin B
C26H42O4 = 418
Synthesis    2014, 46 , 1205
L. Maram, B. Das
DOI: 10.1055/s-0033-1340866
CrossRef
 
chiral
racemic
Notes:


Polyketides
Aculeatin D
C26H42O4 = 418
Synthesis    2014, 46 , 1205
L. Maram, B. Das
DOI: 10.1055/s-0033-1340866
CrossRef
 
chiral
racemic
Notes:


Polyketides
Spirodienal A
C32H54O7 = 550
Angew. Chem. Int. Ed.    2014, 53 , 4915
S. Newton, C. F. Carter, C. M. Pearson, L. C. Alves, H. Lange, P. Thansandote, S. V. Ley
DOI: 10.1002/anie.201402056
CrossRef
 
chiral
racemic
Notes:


Polyketides
Spiragien A
C41H66O9 = 702
Angew. Chem. Int. Ed.    2014, 53 , 4915
S. Newton, C. F. Carter, C. M. Pearson, L. C. Alves, H. Lange, P. Thansandote, S. V. Ley
DOI: 10.1002/anie.201402056
CrossRef
 
chiral
racemic
Notes: formal synthesis


Aromatics
Furomollugin
C14H10O4 = 242
Org. Lett.    2014, 16 , 2490
M. Buccini, M. J. Piggott
DOI: 10.1021/ol500862w
CrossRef
 
chiral
racemic
Notes:


Aromatics
Monosporascone
C13H8O5 = 244
Org. Biomol. Chem.    2014, 12 , 2801
K. A. Punch, M. J. Piggott
DOI: 10.1039/c4ob00331d
CrossRef
 
chiral
racemic
Notes:


Aromatics
Ruscozepine A
C16H14O3 = 254
Eur. J. Org. Chem.    2014, , 3170
J. M. Herrmann, M. Untergehrer, G. Jürgenliemk, J. Heilmann, B. König
DOI: 10.1002/ejoc.201400004
CrossRef
 
chiral
racemic
Notes:


Aromatics
Frutinone A
C16H8O4 = 264
Tetrahedron    2014, 70 , 3452
M. Yoshida, K. Saito, Y. Fujino, T. Doi
DOI: 10.1016/j.tet.2014.03.073
CrossRef
 
chiral
racemic
Notes:


Aromatics
Tanshinone Ⅰ
C18H12O3 = 276
Tetrahedron    2014, 70 , 2976
M. Jiao, C. Ding, A. Zhang
DOI: 10.1016/j.tet.2014.03.019
CrossRef
 
chiral
racemic
Notes:


Aromatics
Frutinone C
C16H8O5 = 280
Tetrahedron    2014, 70 , 3452
M. Yoshida, K. Saito, Y. Fujino, T. Doi
DOI: 10.1016/j.tet.2014.03.073
CrossRef
 
chiral
racemic
Notes:


Aromatics
Ruscozepine B
C17H16O4 = 284
Eur. J. Org. Chem.    2014, , 3170
J. M. Herrmann, M. Untergehrer, G. Jürgenliemk, J. Heilmann, B. König
DOI: 10.1002/ejoc.201400004
CrossRef
 
chiral
racemic
Notes:


Aromatics
Frutinone B
C17H10O5 = 294
Tetrahedron    2014, 70 , 3452
M. Yoshida, K. Saito, Y. Fujino, T. Doi
DOI: 10.1016/j.tet.2014.03.073
CrossRef
 
chiral
racemic
Notes:


Aromatics
Filiformin
C15H19OBr = 295
Angew. Chem. Int. Ed.    2014, 53 , 5552
D. J. Blair, C. J. Fletcher, K. M. P. Wheelhouse, V. K. Aggarwal
DOI: 10.1002/anie.201400944
CrossRef
 
chiral
racemic
Notes:


Aromatics
Chinensin
C21H16O6 = 304
Chem. Commun.    2014, 50 , 5641
Y. He, X. Zhang, X. Fan
DOI: 10.1039/c4cc01738b
CrossRef
 
chiral
racemic
Notes:


Aromatics
Taiwanin C
C20H23O6 = 348
Chem. Commun.    2014, 50 , 5641
Y. He, X. Zhang, X. Fan
DOI: 10.1039/c4cc01738b
CrossRef
 
chiral
racemic
Notes:


Aromatics
Radermachol
C24H16O4 = 368
Org. Lett.    2014, 16 , 2490
M. Buccini, M. J. Piggott
DOI: 10.1021/ol500862w
CrossRef
 
chiral
racemic
Notes:


  76 data found. 1 - 30 listed Next Last   
   
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