Heterocycles Database
Total Synthesis of
Heterocyclic
Natural Products
 
 1975-2012
 19,753 Compounds
 23 January, 2012
 
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 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.
 
23 January, 2012
Search by Group:
Polyketides
Aromatics
Terpenes
Steroids
Alkaloids
Antibiotics
Miscellaneous
 
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Search by Journal :
Vol.
No.
Angew. Chem. Int. Ed.
50
26, 27
Chem. Commun.
47
23
Chem. Eur. J.
17
25
Chem. Pharm. Bull.
59
6
Eur. J. Org. Chem.
2011
16, 17
Helv. Chim. Acta
94
6
J. Am. Chem. Soc.
133
21, 23-25
J. Nat. Prod.
74
6
J. Org. Chem.
76
11, 12
Org. Biomol. Chem.
9
9-12
Org. Lett.
13
11, 12
Synlett
9, 10
Synth. Commun.
41
9
Synthesis
11, 12
Tetrahedron
67
22, 23, 25
Tetrahedron Asymmetry
22
11, 12
Tetrahedron Lett.
52
23-25
  77 data found. 1 - 30 listed Next Last   

Polyketides
Ophiocerin A
C6H12O3 = 132
Tetrahedron Asymmetry    2011, 22 , 1212
K. Show, P. Gupta, P. Kumar
DOI: 10.1016/j.tetasy.2011.06.015
CrossRef
 
chiral
racemic
Notes:


Polyketides
Ophiocerin C
C6H12O3 = 132
Tetrahedron Asymmetry    2011, 22 , 1212
K. Show, P. Gupta, P. Kumar
DOI: 10.1016/j.tetasy.2011.06.015
CrossRef
 
chiral
racemic
Notes:


Polyketides
Brebicomine, Endo-
C9H16O2 = 156
Tetrahedron    2011, 67 , 4036
P. Pal, A. K. Shaw
DOI: 10.1016/j.tet.2011.04.014
CrossRef
 
chiral
racemic
Notes: both enantiomer


Polyketides
Brebicomine, Exo-
C9H16O2 = 156
Tetrahedron    2011, 67 , 4036
P. Pal, A. K. Shaw
DOI: 10.1016/j.tet.2011.04.014
CrossRef
 
chiral
racemic
Notes: both enantiomer


Polyketides
Massoialactone
C10H16O2 = 168
Synthesis    2011, , 1954
A. Harbindu, P. Kumar
DOI: 10.1055/s-0030-1260051
CrossRef
 
chiral
racemic
Notes:


Polyketides
Sapinofuranone B
C10H14O3 = 182
Tetrahedron    2011, 67 , 4620
J. S. Yadav, S. S. Mandal, J. S. S. Reddy, P. Srihari
DOI: 10.1016/j.tet.2011.04.072
CrossRef
 
chiral
racemic
Notes: (+)-enantiomer


Polyketides
Ethisolide
C10H12O4 = 196
Org. Biomol. Chem.    2011, 9 , 4079
G. V. M. Sharma, D. H. Chary, N. Chandramouli, F. Achrainer, S. Patrudu, H. Zipse
DOI: 10.1039/c1ob00019e
CrossRef
 
chiral
racemic
Notes: formal synthesis


Polyketides
Goniothalamin
C13H12O2 = 200
Tetrahedron Asymmetry    2011, 22 , 1249
B. Das, S. Nagendra, C. R. Reddy
DOI: 10.1016/j.tetasy.2011.06.029
CrossRef
 
chiral
racemic
Notes:


Polyketides
Cyclophostin
C8H11O6P = 234
Org. Lett.    2011, 13 , 3094
R. K. Malla, S. Bandyopadhyay, C. D. Spilling, S. Dutta, C. M. Dupureur
DOI: 10.1021/ol200991x
CrossRef
 
chiral
racemic
Notes:


Polyketides
Goniodiol
C13H14O4 = 234
Helv. Chim. Acta    2011, 94 , 1102
P. R. Krishna, M. Alivelu
DOI: 10.1002/hlca.201000365
CrossRef
 
chiral
racemic
Notes:


Polyketides
Asteriscanolide
C15H22O3 = 250
Chem. Commun.    2011, 47 , 6659
Y. Liang, X. Jiang, Z.-X. Yu
DOI: 10.1039/c1cc11005e
CrossRef
 
chiral
racemic
Notes:


Polyketides
Goniofufurone
C13H14O5 = 250
Tetrahedron    2011, 67 , 4036
P. Pal, A. K. Shaw
DOI: 10.1016/j.tet.2011.04.014
CrossRef
 
chiral
racemic
Notes: (+)-enantiomer


Polyketides
Leiocarpin C
C13H16O5 = 252
Helv. Chim. Acta    2011, 94 , 1102
P. R. Krishna, M. Alivelu
DOI: 10.1002/hlca.201000365
CrossRef
 
chiral
racemic
Notes:


Polyketides
Brefeldin C
C16H24O3 = 264
Synlett    2011, , 1459
M. Inai, T. Nishii, S. Mukoujima, T. Esumi, H. Kaku, K. Tominaga, H. Abe, M. Horikawa, T. Tsunoda
DOI: 10.1055/s-0030-1260762
CrossRef
 
chiral
racemic
Notes:


Polyketides
Cardiobutanolide
C13H16O6 = 268
Tetrahedron    2011, 67 , 4036
P. Pal, A. K. Shaw
DOI: 10.1016/j.tet.2011.04.014
CrossRef
 
chiral
racemic
Notes: both enantiomer


Polyketides
Microcarpalide
C16H28O5 = 300
Tetrahedron    2011, 67 , 4268
K. R. Prasad, K. Penchalaiah
DOI: 10.1016/j.tet.2011.03.102
CrossRef
 
chiral
racemic
Notes: (+)-enantiomer


Polyketides
Bovidic Acid
C18H34O4 = 314
Tetrahedron Lett.    2011, 52 , 2943
J. S. Yadav, K. Ramesh, U. V. S. Reddy, B. V. S. Reddy, A. A. K. A. Ghamdi
DOI: 10.1016/j.tetlet.2011.03.089
CrossRef
 
chiral
racemic
Notes:


Polyketides
Cryptofolione
C19H22O4 = 314
Tetrahedron Asymmetry    2011, 22 , 1249
B. Das, S. Nagendra, C. R. Reddy
DOI: 10.1016/j.tetasy.2011.06.029
CrossRef
 
chiral
racemic
Notes:


Polyketides
Macrosphelide A
C16H22O8 = 342
Tetrahedron    2011, 67 , 4512
K. R. Prasad, P. Gutala
DOI: 10.1016/j.tet.2011.04.106
CrossRef
 
chiral
racemic
Notes: (+)-enantiomer


Polyketides
Macrosphelide E
C16H22O8 = 342
Tetrahedron    2011, 67 , 4512
K. R. Prasad, P. Gutala
DOI: 10.1016/j.tet.2011.04.106
CrossRef
 
chiral
racemic
Notes: (+)-enantiomer


Polyketides
Verbalactone
C23H36O6 = 372
Synthesis    2011, , 1954
A. Harbindu, P. Kumar
DOI: 10.1055/s-0030-1260051
CrossRef
 
chiral
racemic
Notes:


Polyketides
Bitungolide E
C25H34O4 = 398
Tetrahedron Lett.    2011, 52 , 3106
J. Shashidhar, K. M. Reddy, S. Ghosh
DOI: 10.1016/j.tetlet.2011.04.008
CrossRef
 
chiral
racemic
Notes:


Polyketides
Okilactomycin
C24H32O6 = 416
Angew. Chem. Int. Ed.    2011, 50 , 5892
J. M. Tenenbaum, W. J. Morris, D. W. Custar, K. A. Scheidt
DOI: 10.1002/anie.201102037
CrossRef
 
chiral
racemic
Notes: (-)-enantiomer


Polyketides
Cyclipostin P
C23H41O6P = 444
Org. Lett.    2011, 13 , 3094
R. K. Malla, S. Bandyopadhyay, C. D. Spilling, S. Dutta, C. M. Dupureur
DOI: 10.1021/ol200991x
CrossRef
 
chiral
racemic
Notes:


Polyketides
Lactimidomycin
C26H35NO6 = 457
J. Am. Chem. Soc.    2011, 133 , 9232
D. Gallenkamp, A. Fürstner
DOI: 10.1021/ja2031085
CrossRef
 
chiral
racemic
Notes: formal synthesis


Polyketides
Iriomoteolide-3a, 7,8-O-Isopropylidene-
C28H42O6 = 474
Org. Biomol. Chem.    2011, 9 , 4518
Y. Zhang, L. Deng, G. Zhao
DOI: 10.1039/c0ob01253j
CrossRef
 
chiral
racemic
Notes:


Polyketides
Leustroducsin B
C34H56NO10P = 669
Org. Lett.    2011, 13 , 3206
S. N. Greszler, J. T. Malinowski, J. S. Johnson
DOI: 10.1021/ol2011192
CrossRef
 
chiral
racemic
Notes: formal synthesis


Polyketides
Iejimalide B
C41H60N2O7 = 692
Chem. Eur. J.    2011, 17 , 6964
J. Gagnepain, E. Moulin, A. Fürstner
DOI: 10.1002/chem.201100178
CrossRef
 
chiral
racemic
Notes:


Polyketides
Dolabelide C
C43H72O13 = 797
J. Org. Chem.    2011, 76 , 4358
P. R. Hanson, R. Chegondi, J. Nguyen, C. D. Thomas, J. D. Waetzig, A. Whitehead
DOI: 10.1021/jo2003506
CrossRef
 
chiral
racemic
Notes:


Polyketides
Cyanolide A
C42H52O16 = 832
J. Am. Chem. Soc.    2011, 133 , 9727
M. R. Gesinski, S. D. Rychnovsky
DOI: 10.1021/ja204228q
CrossRef
 
chiral
racemic
Notes: formal synthesis


  77 data found. 1 - 30 listed Next Last   
   
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