Heterocycles Database
Total Synthesis of
Heterocyclic
Natural Products
 
 1975-2013
 19,943 Compounds
 27 April, 2012
 
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
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
  151 data found. 1 - 30 listed Next Last   

Polyketides
Rengyolone
C8H10O3 = 154
Org. Lett.    2012, 14 , 4537
P. D. Brown, A. C. Willis, M. S. Sherburn, A. L. Lawrence
DOI: 10.1021/ol302042u
CrossRef
 
chiral
racemic
Notes:


Polyketides
Rengyolone
C8H10O3 = 154
Org. Lett.    2012, 14 , 4878
K. Zhao, G.-J. Cheng, H. Yang, H. Shang, X. Zhang, Y.-D. Wu, Y. Tang
DOI: 10.1021/ol302205w
CrossRef
 
chiral
racemic
Notes:


Polyketides
Nectriapyrone
C11H14O3 = 194
Tetrahedron    2012, 68 , 7280
O. Geiseler, J. Podlech
DOI: 10.1016/j.tet.2012.06.104
CrossRef
 
chiral
racemic
Notes:


Polyketides
Trochliophorolide B
C12H14O3 = 206
Org. Lett.    2012, 14 , 4698
B. M. Trost, A. Quintard
DOI: 10.1021/ol302074h
CrossRef
 
chiral
racemic
Notes: total synthesis of the proposed structure


Polyketides
Xylarone, 8,9-Dehydro-
C12H14O3 = 206
Tetrahedron    2012, 68 , 7280
O. Geiseler, J. Podlech
DOI: 10.1016/j.tet.2012.06.104
CrossRef
 
chiral
racemic
Notes:


Polyketides
Aplysiopsene A
C12H16O3 = 208
Tetrahedron    2012, 68 , 7280
O. Geiseler, J. Podlech
DOI: 10.1016/j.tet.2012.06.104
CrossRef
 
chiral
racemic
Notes:


Polyketides
Helicascolide C
C12H18O3 = 210
Tetrahedron Lett.    2012, 53 , 4997
P. R. Krishna, V. S. Mallula, P. V. A. Kumar
DOI: 10.1016/j.tetlet.2012.07.018
CrossRef
 
chiral
racemic
Notes:


Polyketides
Umuravumbolide, Deacetyl-
C12H18O3 = 210
Helv. Chim. Acta    2012, 95 , 1593
V. Shekhar, D. K. Reddy, Y. Venkateswarlu
DOI: 10.1002/hlca.201200078
CrossRef
 
chiral
racemic
Notes:


Polyketides
Helicascolide A
C12H20O3 = 212
Tetrahedron Lett.    2012, 53 , 4997
P. R. Krishna, V. S. Mallula, P. V. A. Kumar
DOI: 10.1016/j.tetlet.2012.07.018
CrossRef
 
chiral
racemic
Notes:


Polyketides
Patulolide C
C12H20O3 = 212
Org. Biomol. Chem.    2012, 10 , 6995
E. K. Hoegenauer, E. J. Thomas
DOI: 10.1039/c2ob25992c
CrossRef
 
chiral
racemic
Notes:


Polyketides
Patulolide C, epi-
C12H20O3 = 212
Org. Biomol. Chem.    2012, 10 , 6995
E. K. Hoegenauer, E. J. Thomas
DOI: 10.1039/c2ob25992c
CrossRef
 
chiral
racemic
Notes:


Polyketides
Aplysiopsene B
C13H18O3 = 222
Tetrahedron    2012, 68 , 7280
O. Geiseler, J. Podlech
DOI: 10.1016/j.tet.2012.06.104
CrossRef
 
chiral
racemic
Notes:


Polyketides
Aplysiopsene C
C13H18O3 = 222
Tetrahedron    2012, 68 , 7280
O. Geiseler, J. Podlech
DOI: 10.1016/j.tet.2012.06.104
CrossRef
 
chiral
racemic
Notes:


Polyketides
Mycosporulone
C11H10O5 = 222
Org. Lett.    2012, 14 , 4898
M. E. Jung, J. J. Chang
DOI: 10.1021/ol302234a
CrossRef
 
chiral
racemic
Notes: total synthesis of the proposed structure


Polyketides
Phomapyrone D
C12H14O4 = 222
Tetrahedron    2012, 68 , 7280
O. Geiseler, J. Podlech
DOI: 10.1016/j.tet.2012.06.104
CrossRef
 
chiral
racemic
Notes:


Polyketides
Phomapyrone A
C14H18O3 = 234
Tetrahedron    2012, 68 , 7280
O. Geiseler, J. Podlech
DOI: 10.1016/j.tet.2012.06.104
CrossRef
 
chiral
racemic
Notes:


Polyketides
Aplysiopsene D
C14H20O3 = 236
Tetrahedron    2012, 68 , 7280
O. Geiseler, J. Podlech
DOI: 10.1016/j.tet.2012.06.104
CrossRef
 
chiral
racemic
Notes:


Polyketides
Umuravumbolide
C14H20O4 = 252
Helv. Chim. Acta    2012, 95 , 1593
V. Shekhar, D. K. Reddy, Y. Venkateswarlu
DOI: 10.1002/hlca.201200078
CrossRef
 
chiral
racemic
Notes:


Polyketides
Infectopyrone
C14H16O5 = 264
Tetrahedron    2012, 68 , 7280
O. Geiseler, J. Podlech
DOI: 10.1016/j.tet.2012.06.104
CrossRef
 
chiral
racemic
Notes:


Polyketides
Cryptocaryanone A
C17H14O4 = 282
Synlett    2012, 23 , 2129
B. Zhang, Z. Yang, G. Zhao, B. Ma, X. Xie, X. She
DOI: 10.1055/s-0032-1316580
CrossRef
 
chiral
racemic
Notes:


Polyketides
Phomopsolide B
C15H20O6 = 296
Tetrahedron    2012, 68 , 7489
K. R. Prasad, P. Gutala
DOI: 10.1016/j.tet.2012.06.002
CrossRef
 
chiral
racemic
Notes:


Polyketides
Incarviditone
C16H20O6 = 308
Org. Lett.    2012, 14 , 4537
P. D. Brown, A. C. Willis, M. S. Sherburn, A. L. Lawrence
DOI: 10.1021/ol302042u
CrossRef
 
chiral
racemic
Notes:


Polyketides
Incarviditone
C16H20O6 = 308
Org. Lett.    2012, 14 , 4878
K. Zhao, G.-J. Cheng, H. Yang, H. Shang, X. Zhang, Y.-D. Wu, Y. Tang
DOI: 10.1021/ol302205w
CrossRef
 
chiral
racemic
Notes:


Polyketides
Incarvilleatone
C16H20O6 = 308
Org. Lett.    2012, 14 , 4537
P. D. Brown, A. C. Willis, M. S. Sherburn, A. L. Lawrence
DOI: 10.1021/ol302042u
CrossRef
 
chiral
racemic
Notes:


Polyketides
Incarvilleatone
C16H20O6 = 308
Org. Lett.    2012, 14 , 4878
K. Zhao, G.-J. Cheng, H. Yang, H. Shang, X. Zhang, Y.-D. Wu, Y. Tang
DOI: 10.1021/ol302205w
CrossRef
 
chiral
racemic
Notes:


Polyketides
Seimatopolide A
C18H32O5 = 328
Eur. J. Org. Chem.    2012, , 4910
C. R. Reddy, N. N. Rao, M. D. Reddy
DOI: 10.1002/ejoc.201200732
CrossRef
 
chiral
racemic
Notes:


Polyketides
Sch 725680
C21H22O7 = 386
Org. Lett.    2012, 14 , 4303
T. Takeuchi, Y. Mizushina, S. Takaichi, N. Inoue, K. Kuramochi, S. Shimura, Y. Myobatake, Y. Katayama, K. Takemoto, S. Endo, S. Kamisuki, F. Sugawara
DOI: 10.1021/ol301865u
CrossRef
 
chiral
racemic
Notes:


Polyketides
Aureothin
C22H23NO6 = 397
Angew. Chem. Int. Ed.    2012, 51 , 9587
M. Henrot, M. E. A. Richter, J. Maddaluno, C. Hertweck, Michaël De Paolis
DOI: 10.1002/anie.201204259
CrossRef
 
chiral
racemic
Notes:


Polyketides
Ripostatin A
C30H38O6 = 494
Org. Lett.    2012, 14 , 4690
W. Tang, E. V. Prusov
DOI: 10.1021/ol302219x
CrossRef
 
chiral
racemic
Notes:


Polyketides
Dictyostatin
C32H52O6 = 532
Chem. Eur. J.    2012, 18 , 11788
J. Gallon, J. Esteban, S. Bouzbouz, M. Campbell, S. Reymond, J. Cossy
DOI: 10.1002/chem.201201001
CrossRef
 
chiral
racemic
Notes: formal synthesis


  151 data found. 1 - 30 listed Next Last   
   
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