Heterocycles Database
Total Synthesis of
Heterocyclic
Natural Products
 
 1975-2014
 19,943 Compounds
 27 April, 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.
 
27 April, 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
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
  65 data found. 1 - 30 listed Next Last   

Polyketides
Brevicomin, exo-
C9H16O2 = 156
Helv. Chim. Acta    2013, 96 , 1610
G. Sabitha, A. M. Reddy, S. S. S. Reddy, J. S. Yadav
DOI: 10.1002/hlca.201200611
CrossRef
 
chiral
racemic
Notes:


Polyketides
No Name
C10H12O2 = 164
Eur. J. Org. Chem.    2013, , 2906
S. M. Wickel, C. A. Citron, J. S. Dickschat
DOI: 10.1002/ejoc.201300049
CrossRef
 
chiral
racemic
Notes:


Polyketides
No Name
C10H14O2 = 166
Eur. J. Org. Chem.    2013, , 2906
S. M. Wickel, C. A. Citron, J. S. Dickschat
DOI: 10.1002/ejoc.201300049
CrossRef
 
chiral
racemic
Notes:


Polyketides
No Name
C10H16O2 = 168
Eur. J. Org. Chem.    2013, , 2906
S. M. Wickel, C. A. Citron, J. S. Dickschat
DOI: 10.1002/ejoc.201300049
CrossRef
 
chiral
racemic
Notes:


Polyketides
Brevicomin, 1-Hydroxy-exo-
C9H16O3 = 172
Helv. Chim. Acta    2013, 96 , 1610
G. Sabitha, A. M. Reddy, S. S. S. Reddy, J. S. Yadav
DOI: 10.1002/hlca.201200611
CrossRef
 
chiral
racemic
Notes:


Polyketides
Cyclophellitol
C7H12O5 = 176
J. Org. Chem.    2013, 78 , 7690
S. Mondal, A. Prathap, K. M. Sureshan
DOI: 10.1021/jo401272j
CrossRef
 
chiral
racemic
Notes:


Polyketides
Ieodomycin B
C12H18O3 = 210
Tetrahedron Lett.    2013, 54 , 4544
N. N. Rao, H. M. Meshram
DOI: 10.1016/j.tetlet.2013.06.071
CrossRef
 
chiral
racemic
Notes:


Polyketides
Umuravumbolide, Desacetyl-
C12H18O3 = 210
Tetrahedron Asymmetry    2013, 24 , 594
T. V. Kumar, G. V. Reddy, K. S. Babu, J. M. Rao
DOI: 10.1016/j.tetasy.2013.04.004
CrossRef
 
chiral
racemic
Notes:


Polyketides
Umuravumbolide
C14H20O4 = 252
Tetrahedron Asymmetry    2013, 24 , 594
T. V. Kumar, G. V. Reddy, K. S. Babu, J. M. Rao
DOI: 10.1016/j.tetasy.2013.04.004
CrossRef
 
chiral
racemic
Notes:


Polyketides
Hyperolactone C
C16H14O4 = 270
Org. Biomol. Chem.    2013, 11 , 5362
D. M. Hodgson, E. Moreno-Clavijo, S. E. Day, S. Man
DOI: 10.1039/c3ob41251b
CrossRef
 
chiral
racemic
Notes:


Polyketides
Synargentolide B
C16H22O8 = 342
Eur. J. Org. Chem.    2013, , 4870
G. Sabitha, K. Shankaraiah, J. S. Yadav
DOI: 10.1002/ejoc.201300434
CrossRef
 
chiral
racemic
Notes:


Polyketides
Alternaric Acid
C21H30O8 = 410
Chem. Commun.    2013, 49 , 7001
R. Nagase, Y. Oguni, S. Ureshino, H. Mura, T. Misaki, Y. Tanabe
DOI: 10.1039/c3cc43180k
CrossRef
 
chiral
racemic
Notes:


Polyketides
Platensimycin
C24H27NO7 = 441
J. Org. Chem.    2013, 78 , 7912
L. Zhu, C. Zhou, W. Yang, S. He, G.-J. Cheng, X. Zhang, C.-S. Lee
DOI: 10.1021/jo401105q
CrossRef
 
chiral
racemic
Notes: formal synthesis


Polyketides
Spongistatin 2
C63H96O21 = 1188
Chem. Sci.    2013, 4 , 1989
H. Kraus, A. Francais, M. O’Brien, J. Frost, A. Diéguez-Vàzquez, A. Polara, N. Baricordi, R. Horan, D.-S. Hsu, T. Tsunoda, S. V. Ley
DOI: 10.1039/c3sc50304f
CrossRef
 
chiral
racemic
Notes:


Aromatics
Cladosporin
C16H20O5 = 292
Eur. J. Org. Chem.    2013, , 2859
D. K. Mohapatra, S. Maity, T. S. Rao, J. S. Yadav, B. Sridhar
DOI: 10.1002/ejoc.201300053
CrossRef
 
chiral
racemic
Notes: formal synthesis


Aromatics
Harringtonolide
C19H18O4 = 310
J. Am. Chem. Soc.    2013, 135 , 12434
M. Zhang, N. Liu, W. Tang
DOI: 10.1021/ja406255j
CrossRef
 
chiral
racemic
Notes:


Aromatics
Hainanolidol
C19H20O4 = 312
J. Am. Chem. Soc.    2013, 135 , 12434
M. Zhang, N. Liu, W. Tang
DOI: 10.1021/ja406255j
CrossRef
 
chiral
racemic
Notes:


Aromatics
Deguelin
C23H22O6 = 394
Chem. Sci.    2013, 4 , 3304
R. L. Farmer, K. A. Scheidt
DOI: 10.1039/c3sc50424g
CrossRef
 
chiral
racemic
Notes:


Aromatics
Cavicularin
C28H22O4 = 422
Tetrahedron    2013, 69 , 6959
K. Harada, K. Makino, N. Shima, H. Okuyama, T. Esumi, M. Kubo, H. Hioki, Y. Asakawa, Y. Fukuyama
DOI: 10.1016/j.tet.2013.06.064
CrossRef
 
chiral
racemic
Notes:


Aromatics
Riccardin C
C28H24O4 = 424
Tetrahedron    2013, 69 , 6959
K. Harada, K. Makino, N. Shima, H. Okuyama, T. Esumi, M. Kubo, H. Hioki, Y. Asakawa, Y. Fukuyama
DOI: 10.1016/j.tet.2013.06.064
CrossRef
 
chiral
racemic
Notes:


Alkaloids
Coniine
C8H17N = 127
Eur. J. Org. Chem.    2013, , 5464
V. H. Vu, L.-A. Jouanno, A. Cheignon, T. Roisnel, V. Dorcet, S. Sinbandhit, J.-P. Hurvois
DOI: 10.1002/ejoc.201300595
CrossRef
 
chiral
racemic
Notes:


Alkaloids
Pipecolic Acid, 3,4-Dihydroxy-
C6H11NO4 = 161
J. Org. Chem.    2013, 78 , 7406
K. S. A. Kumar, J. S. Rathee, M. Subramanian, S. Chattopadhyay
DOI: 10.1021/jo400448p
CrossRef
 
chiral
racemic
Notes:


Alkaloids
Mannojirimycin, 1-Deoxy-
C6H13NO4 = 163
Eur. J. Org. Chem.    2013, , 5149
J. Hoecker, G. C. Rudolf, F. Bächle, S. Fleischer, B. D.Lindner, G. Helmchen
DOI: 10.1002/ejoc.201300445
CrossRef
 
chiral
racemic
Notes:


Alkaloids
Penmacric Acid
C7H10N2O5 = 202
Tetrahedron    2013, 69 , 6866
M. Ueda, A. Ono, D. Nakao, K. Matsuno, T. Naito, O. Miyata
DOI: 10.1016/j.tet.2013.06.006
CrossRef
 
chiral
racemic
Notes: Total synthesis of its three epimer were accomplished.


Alkaloids
Salsolidine
C12H17NO2 = 207
Tetrahedron Lett.    2013, 54 , 4228
N. S. S. Reddy, B. J. M. Reddy, B. V. S. Reddy
DOI: 10.1016/j.tetlet.2013.05.132
CrossRef
 
chiral
racemic
Notes:


Alkaloids
Crispine A
C14H19NO2 = 233
Tetrahedron Lett.    2013, 54 , 4228
N. S. S. Reddy, B. J. M. Reddy, B. V. S. Reddy
DOI: 10.1016/j.tetlet.2013.05.132
CrossRef
 
chiral
racemic
Notes:


Alkaloids
Benzo[a]quinolizidine
C15H21NO2 = 247
Tetrahedron Lett.    2013, 54 , 4228
N. S. S. Reddy, B. J. M. Reddy, B. V. S. Reddy
DOI: 10.1016/j.tetlet.2013.05.132
CrossRef
 
chiral
racemic
Notes:


Alkaloids
Rigidiusculamide A
C13H17NO4 = 251
Helv. Chim. Acta    2013, 96 , 1564
P. R. Krishna, B. K. Reddy
DOI: 10.1002/hlca.201200598
CrossRef
 
chiral
racemic
Notes: Synthesis of the originally proposed structure


Alkaloids
Solenopsin A
C17H35N = 253
Eur. J. Org. Chem.    2013, , 5464
V. H. Vu, L.-A. Jouanno, A. Cheignon, T. Roisnel, V. Dorcet, S. Sinbandhit, J.-P. Hurvois
DOI: 10.1002/ejoc.201300595
CrossRef
 
chiral
racemic
Notes:


Alkaloids
Higenamine
C16H17NO3 = 271
Eur. J. Org. Chem.    2013, , 2898
H.-P. Wu, T.-N. Lu, N.-Y. Hsu, C.-C. Chang
DOI: 10.1002/ejoc.201300072
CrossRef
 
chiral
racemic
Notes: synthesis of the enantiomer


  65 data found. 1 - 30 listed Next Last   
   
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