Heterocycles Database
Total Synthesis of
Heterocyclic
Natural Products
 
 1975-2010
 18,479 Compounds
 26 July, 2010
 
Search by:
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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
Hayato Fukuda
Naoki Kanoh
Muneo Kawasumi
Yusuke Sasano
Masatoshi Sibuya
Hiroyuki Yamakoshi

Editorial Assistants
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.
 
26 July, 2010
Search by Group:
Polyketides
Aromatics
Terpenes
Steroids
Alkaloids
Antibiotics
Miscellaneous
 
All
 
Search by Journal :
Vol.
No.
Angew. Chem. Int. Ed.
49
2,4,5
Chem. Commun.
2010
1
Chem. Eur. J.
16
1,2,4
Eur. J. Org. Chem.
2010
2
Helv. Chim. Acta
93
1
Heterocycles
81
1
J. Am. Chem. Soc.
132
1
J. Org. Chem.
75
1,2
Org. Biomol. Chem.
8
1,2
Synlett
2010
1,2
Synthesis
2010
1
Tetrahedron
66
1,2,4
Tetrahedron Asymmetry
21
1
Tetrahedron Lett.
51
1-4
  62 data found. 1 - 30 listed Next Last   

Polyketides
Brevicomin, Iso-exo-
C9H1O2 = 156
Synlett    2010, , 207
A. Bouziane, T. Régnier, F. Carreaux, B. Carboni, C. Bruneau, J.-L. Renaud
DOI: 10.1055/s-0029-1218561
CrossRef
 
chiral
racemic
Notes:


Polyketides
Cephalosporolide E
C10H14O4 = 198
Synlett    2010, , 158
R. A. Fernandes, A. B. Ingle
DOI: 10.1055/s-0029-1218538
CrossRef
 
chiral
racemic
Notes:


Polyketides
Cephalosporolide F
C10H14O4 = 198
Synlett    2010, , 158
R. A. Fernandes, A. B. Ingle
DOI: 10.1055/s-0029-1218538
CrossRef
 
chiral
racemic
Notes:


Polyketides
Decarestrictine J
C10H16O4 = 200
Tetrahedron    2010, 66 , 334
J. S. Yadav, K. A. Lakshmi, N. M. Reddy, A. R. Prasad, B. V. S. Reddy
DOI: 10.1016/j.tet.2009.10.100
CrossRef
 
chiral
racemic
Notes:


Polyketides
No Name
C13H20O3 = 224
Tetrahedron    2010, 66 , 187
Y. Wang, W.-Min. Dai
DOI: 10.1016/j.tet.2009.10.115
CrossRef
 
chiral
racemic
Notes:


Polyketides
No Name
C13H20O3 = 224
Tetrahedron    2010, 66 , 187
Y. Wang, W.-Min. Dai
DOI: 10.1016/j.tet.2009.10.115
CrossRef
 
chiral
racemic
Notes:


Polyketides
Laurepan, Iso-
C15H30O = 226
Org. Biomol. Chem.    2010, 8 , 39
M. Ebine, Y. Suga, H. Fuwa, M. Sasaki
DOI: 10.1039/b919673k
CrossRef
 
chiral
racemic
Notes:


Polyketides
No Name
C13H22O3 = 226
Tetrahedron    2010, 66 , 187
Y. Wang, W.-Min. Dai
DOI: 10.1016/j.tet.2009.10.115
CrossRef
 
chiral
racemic
Notes:


Polyketides
No Name
C13H22O3 = 226
Tetrahedron    2010, 66 , 187
Y. Wang, W.-Min. Dai
DOI: 10.1016/j.tet.2009.10.115
CrossRef
 
chiral
racemic
Notes:


Polyketides
Stagonolide A
C12H18O4 = 226
Tetrahedron Asymmetry    2010, 21 , 106
P. Srihari, B. Kumaraswamy, G. M. Rao, J. S. Yadav
DOI: 10.1016/j.tetasy.2009.12.015
CrossRef
 
chiral
racemic
Notes:


Polyketides
No Name
C12H20O4 = 228
Synthesis    2010, , 73
J. S. Yadav, N. Thrimurtulu, M. Venkatesh, K. V. R. Rao, A. R. Prasad, B. V. S. Reddy
DOI: 10.1055/s-0029-1217107
CrossRef
 
chiral
racemic
Notes:


Polyketides
Stagonolide B
C12H20O5 = 244
Org. Biomol. Chem.    2010, 8 , 398
A. G. Giri, M. A. Mondal, V. G. Puranik, C. V. Ramana
DOI: 10.1039/b916198h
CrossRef
 
chiral
racemic
Notes:


Polyketides
Stagonolide B, 4-epi-
C12H20O5 = 244
Org. Biomol. Chem.    2010, 8 , 398
A. G. Giri, M. A. Mondal, V. G. Puranik, C. V. Ramana
DOI: 10.1039/b916198h
CrossRef
 
chiral
racemic
Notes:


Polyketides
Sawaranospirolide C
C14H16O7 = 296
Org. Biomol. Chem.    2010, 8 , 226
J. Robertson, P. T. Chovatia, T. G. Fowler, J. M. Withey, D. J. Woollaston
DOI: 10.1039/b918091e
CrossRef
 
chiral
racemic
Notes: synthesis of enantiomer


Polyketides
Sawaranospirolide D
C14H16O7 = 296
Org. Biomol. Chem.    2010, 8 , 226
J. Robertson, P. T. Chovatia, T. G. Fowler, J. M. Withey, D. J. Woollaston
DOI: 10.1039/b918091e
CrossRef
 
chiral
racemic
Notes: synthesis of enantiomer


Polyketides
Aculeatin E
C24H38O4 = 390
Tetrahedron    2010, 66 , 390
C. V. Ramana, S. K. Pandey
DOI: 10.1016/j.tet.2009.10.058
CrossRef
 
chiral
racemic
Notes:


Polyketides
Aculeatin F
C24H38O4 = 390
Tetrahedron    2010, 66 , 390
C. V. Ramana, S. K. Pandey
DOI: 10.1016/j.tet.2009.10.058
CrossRef
 
chiral
racemic
Notes:


Polyketides
Itomanallene A
C15H20Br2O2 = 390
Angew. Chem. Int. Ed.    2010, 49 , 752
W. Jeong, M. J. Kim, H. Kim, S. Kim, D. Kim, K. J. Shin
DOI: 10.1002/anie.200905826
CrossRef
 
chiral
racemic
Notes: revised structure


Polyketides
Laurallene, Neo-
C15H20Br2O2 = 390
Angew. Chem. Int. Ed.    2010, 49 , 752
W. Jeong, M. J. Kim, H. Kim, S. Kim, D. Kim, K. J. Shin
DOI: 10.1002/anie.200905826
CrossRef
 
chiral
racemic
Notes: systhesis of enantiomer


Polyketides
Aculeatin A
C26H42O4 = 418
Tetrahedron    2010, 66 , 390
C. V. Ramana, S. K. Pandey
DOI: 10.1016/j.tet.2009.10.058
CrossRef
 
chiral
racemic
Notes:


Polyketides
Aculeatin B
C26H42O4 = 418
Tetrahedron    2010, 66 , 390
C. V. Ramana, S. K. Pandey
DOI: 10.1016/j.tet.2009.10.058
CrossRef
 
chiral
racemic
Notes:


Polyketides
Aculeatin D
C26H42O4 = 418
Synlett    2010, , 51
J. S. Yadav, K. V. R. Rao, K. Ravindar, B. V. S. Reddy
DOI: 10.1055/s-0029-1218546
CrossRef
 
chiral
racemic
Notes:


Polyketides
Kendomycin
C29H42O6 = 486
Chem. Eur. J.    2010, 16 , 507
T. Magauer, H. J. Martin, J. Mulzer
DOI: 10.1002/chem.200902226
CrossRef
 
chiral
racemic
Notes:


Aromatics
Equol
C15H14O3 = 242
Tetrahedron    2010, 66 , 197
Y. Takashima, Y. Kaneko, Y. Kobayashi
DOI: 10.1016/j.tet.2009.10.116
CrossRef
 
chiral
racemic
Notes:


Aromatics
Ptaeroxylin
C15H14O4 = 258
J. Org. Chem.    2010, 75 , 353
M. Bruder, P. L. Haseler, M. Muscarella, W. Lewis, C. J. Moody
DOI: 10.1021/jo902117e
CrossRef
 
chiral
racemic
Notes: desoxykarenin


Aromatics
Vestitol
C16H16O4 = 272
Tetrahedron    2010, 66 , 197
Y. Takashima, Y. Kaneko, Y. Kobayashi
DOI: 10.1016/j.tet.2009.10.116
CrossRef
 
chiral
racemic
Notes:


Aromatics
Eranthin
C15H14O5 = 274
J. Org. Chem.    2010, 75 , 353
M. Bruder, P. L. Haseler, M. Muscarella, W. Lewis, C. J. Moody
DOI: 10.1021/jo902117e
CrossRef
 
chiral
racemic
Notes:


Aromatics
Ptaeroxylinol
C15H14O5 = 274
J. Org. Chem.    2010, 75 , 353
M. Bruder, P. L. Haseler, M. Muscarella, W. Lewis, C. J. Moody
DOI: 10.1021/jo902117e
CrossRef
 
chiral
racemic
Notes:


Aromatics
Sativan
C17H18O4 = 286
Tetrahedron    2010, 66 , 197
Y. Takashima, Y. Kaneko, Y. Kobayashi
DOI: 10.1016/j.tet.2009.10.116
CrossRef
 
chiral
racemic
Notes:


Aromatics
Centrolobine
C20H24O3 = 312
Tetrahedron Asymmetry    2010, 21 , 103
C. R. Reddy, P. P. Madhavi S. Chandrasekhar
DOI: 10.1016/j.tetasy.2010.01.002
CrossRef
 
chiral
racemic
Notes:


  62 data found. 1 - 30 listed Next Last   
   
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