Heterocycles Database
Total Synthesis of
Heterocyclic
Natural Products
 
 1975-2014
 19,943 Compounds
 27 April, 2012
 
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Journal
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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
  61 data found. 1 - 30 listed Next Last   

Polyketides
Civet
C8H14O3 = 158
J. Org. Chem.    2013, 78 , 12182
S. Sultana, K. Indukuri, M. J. Deka, A. K. Saikia
DOI: 10.1021/jo4015547
CrossRef
 
chiral
racemic
Notes:


Polyketides
Versicolactone A
C8H10O4 = 170
Tetrahedron Lett.    2013, 54 , 6729
L. Wang, W. Zhu
DOI: 10.1016/j.tetlet.2013.09.120
CrossRef
 
chiral
racemic
Notes: synthesis of proposed structure
synthesis of revised structure


Polyketides
Versicolactone B
C8H10O4 = 170
Tetrahedron Lett.    2013, 54 , 6729
L. Wang, W. Zhu
DOI: 10.1016/j.tetlet.2013.09.120
CrossRef
 
chiral
racemic
Notes: synthesis of proposed structure
synthesis of revised structure


Polyketides
Altholactone, Iso-
C13H12O4 = 232
J. Org. Chem.    2013, 78 , 11807
L. Nicolas, E. Izquierdo, P. Angibaud, I. Stansfield, L. Meerpoel, S. Reymond, J. Cossy
DOI: 10.1021/jo401845q
CrossRef
 
chiral
racemic
Notes:


Polyketides
Leiocarpin C
C13H16O5 = 252
Helv. Chim. Acta    2013, 96 , 2179
D. C. Rao, V. Shekhar, D. K. Reddy, B. Chinnababu, Y. Venkateswarlu
DOI: 10.1002/hlca.201200656
CrossRef
 
chiral
racemic
Notes:


Polyketides
Ecklonialactone B
C18H28O3 = 292
Org. Lett.    2013, 15 , 5982
J. Becker, L. Butt, V. von Kiedrowski, E. Mischler, F. Quentin, M. Hiersemann
DOI: 10.1021/ol4028418
CrossRef
 
chiral
racemic
Notes:


Polyketides
Indoxamycin A
C22H30O3 = 342
Angew. Chem. Int. Ed.    2013, 52 , 13256
C. He, C. Zhu, Z. Dai, C.-C. Tseng, H. Ding
DOI: 10.1002/anie.201307426
CrossRef
 
chiral
racemic
Notes: Synthesis of revised structure


Polyketides
Topsentolide C2
C21H34O4 = 350
Tetrahedron Lett.    2013, 54 , 6878
R. Towada, Y. Kurashina, S. Kuwahara
DOI: 10.1016/j.tetlet.2013.10.032
CrossRef
 
chiral
racemic
Notes:


Polyketides
Indoxamycin C
C22H30O4 = 358
Angew. Chem. Int. Ed.    2013, 52 , 13256
C. He, C. Zhu, Z. Dai, C.-C. Tseng, H. Ding
DOI: 10.1002/anie.201307426
CrossRef
 
chiral
racemic
Notes: Synthesis of revised structure


Polyketides
Indoxamycin F
C22H30O4 = 358
Angew. Chem. Int. Ed.    2013, 52 , 13256
C. He, C. Zhu, Z. Dai, C.-C. Tseng, H. Ding
DOI: 10.1002/anie.201307426
CrossRef
 
chiral
racemic
Notes: Synthesis of revised structure


Polyketides
Crassalactone A
C22H20O6 = 380
Helv. Chim. Acta    2013, 96 , 2233
J. S. Yadav, G. M. Rao, B. Thirupathaiah
DOI: 10.1002/hlca.201300231
CrossRef
 
chiral
racemic
Notes:


Aromatics
Lantalucratin B
C15H12O4 = 256
Tetrahedron    2013, 69 , 10470
T. Ogata, Y. Sugiyama, S. Ito, K. Nakano, E. Torii, A. Nishiuchi, T. Kimachi
DOI: 10.1016/j.tet.2013.09.081
CrossRef
 
chiral
racemic
Notes:


Aromatics
Lantalucratin A
C16H14O4 = 270
Tetrahedron    2013, 69 , 10470
T. Ogata, Y. Sugiyama, S. Ito, K. Nakano, E. Torii, A. Nishiuchi, T. Kimachi
DOI: 10.1016/j.tet.2013.09.081
CrossRef
 
chiral
racemic
Notes:


Aromatics
Nigricanin
C15H10O6 = 286
Heterocycles    2013, 87 , 2555
T. Matsukihira, T. Kida, K. Hidaka, S. Saga, M. Takemura, A. Yonoki, T. Nishimori, Y. Horino, T. Harayama, Y. Takeuchi, H. Abe
DOI: 10.3987/COM-13-12847
CrossRef
 
chiral
racemic
Notes:


Aromatics
Monocerin, (12R)-12-Hydroxy-
C16H20O7 = 324
Tetrahedron    2013, 69 , 11025
B. Fang, X. Xie, P. Jing, C. Zhao, H. Li, H. Ma, X. She
DOI: 10.1016/j.tet.2013.09.075
CrossRef
 
chiral
racemic
Notes:


Aromatics
Monocerin, (12S)-12-Hydroxy-
C16H20O7 = 324
Tetrahedron    2013, 69 , 11025
B. Fang, X. Xie, P. Jing, C. Zhao, H. Li, H. Ma, X. She
DOI: 10.1016/j.tet.2013.09.075
CrossRef
 
chiral
racemic
Notes:


Aromatics
Prodelphinidin B3
C30H26O13 = 594
Tetrahedron Lett.    2013, 54 , 7188
W. Fujii, K. Toda, K. Matsumoto, K. Kawaguchi, S. Kawahara, Y. Hattori, H. Fujii, H. Makabe
DOI: 10.1016/j.tetlet.2013.10.113
CrossRef
 
chiral
racemic
Notes:


Aromatics
Prodelphinidin B1
C30H26O14 = 610
Tetrahedron Lett.    2013, 54 , 7188
W. Fujii, K. Toda, K. Matsumoto, K. Kawaguchi, S. Kawahara, Y. Hattori, H. Fujii, H. Makabe
DOI: 10.1016/j.tetlet.2013.10.113
CrossRef
 
chiral
racemic
Notes:


Aromatics
Prodelphinidin B2
C30H26O14 = 610
Tetrahedron Lett.    2013, 54 , 7188
W. Fujii, K. Toda, K. Matsumoto, K. Kawaguchi, S. Kawahara, Y. Hattori, H. Fujii, H. Makabe
DOI: 10.1016/j.tetlet.2013.10.113
CrossRef
 
chiral
racemic
Notes:


Alkaloids
α-Conhydrine
C8H17NO = 143
Tetrahedron    2013, 69 , 10876
C. Bhat, S. G. Tilve
DOI: 10.1016/j.tet.2013.10.082
CrossRef
 
chiral
racemic
Notes: Formal synthesis


Alkaloids
β-Conhydrine
C8H17NO = 143
Tetrahedron    2013, 69 , 10876
C. Bhat, S. G. Tilve
DOI: 10.1016/j.tet.2013.10.082
CrossRef
 
chiral
racemic
Notes: Formal synthesis


Alkaloids
Lentiginosine
C8H15NO2 = 157
Tetrahedron    2013, 69 , 10876
C. Bhat, S. G. Tilve
DOI: 10.1016/j.tet.2013.10.082
CrossRef
 
chiral
racemic
Notes: Formal synthesis


Alkaloids
195C
C13H25N = 195
Tetrahedron    2013, 69 , 10311
X. Wang, J. Li, R. A. Saporito, N. Toyooka
DOI: 10.1016/j.tet.2013.10.009
CrossRef
 
chiral
racemic
Notes: Synthesis of both enantiomers


Alkaloids
Calyxamine A
C12H21NO = 195
Tetrahedron Lett.    2013, 54 , 6852
R.-L. Meza-León, A. Dávila-García, F. Sartillo-Piscil, L. Quintero, M. S. Rivadeneyra, S. Cruz-Gregorio
DOI: 10.1016/j.tetlet.2013.10.022
CrossRef
 
chiral
racemic
Notes:


Alkaloids
Calyxamine B
C12H21NO = 195
Tetrahedron Lett.    2013, 54 , 6852
R.-L. Meza-León, A. Dávila-García, F. Sartillo-Piscil, L. Quintero, M. S. Rivadeneyra, S. Cruz-Gregorio
DOI: 10.1016/j.tetlet.2013.10.022
CrossRef
 
chiral
racemic
Notes:


Alkaloids
Lepadin B
C18H31NO = 277
Chem. Commun.    2013, 49 , 11032
M. Amat, A. Pinto, R. Griera, J. Bosch
DOI: 10.1039/c3cc46801a
CrossRef
 
chiral
racemic
Notes:


Alkaloids
Mersicarpine
C17H20N2O2 = 284
J. Am. Chem. Soc.    2013, 135 , 19127
Z. Xu, Q. Wang, J. Zhu
DOI: 10.1021/ja4115192
CrossRef
 
chiral
racemic
Notes:


Alkaloids
Brunsvigine
C16H17NO4 = 287
Angew. Chem. Int. Ed.    2013, 52 , 14167
X. Bao, Y.-X. Cao, W.-D. Chu, H. Qu, J.-Y. Du, X.-H. Zhao, X.-Y. Ma, C.-T. Wang, C.-A. Fan
DOI: 10.1002/anie.201307324
CrossRef
 
chiral
racemic
Notes:


Alkaloids
Gephyrotoxin 287C
C19H29NO = 287
J. Org. Chem.    2013, 78 , 12532
S. Pichette, D. K. Winter, J. Lessard, C. Spino
DOI: 10.1021/jo402217e
CrossRef
 
chiral
racemic
Notes: formal synthesis


Alkaloids
Pancracine
C16H17NO4 = 287
Angew. Chem. Int. Ed.    2013, 52 , 14167
X. Bao, Y.-X. Cao, W.-D. Chu, H. Qu, J.-Y. Du, X.-H. Zhao, X.-Y. Ma, C.-T. Wang, C.-A. Fan
DOI: 10.1002/anie.201307324
CrossRef
 
chiral
racemic
Notes:


  61 data found. 1 - 30 listed Next Last   
   
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