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
 
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
  63 data found. 1 - 30 listed Next Last   

Polyketides
Telfairic Anhydride, 2,3-Didehydro-
C12H12O5 = 236
J. Org. Chem.    2014, 79 , 2538
P. S. Deore, N. P. Argade
DOI: 10.1021/jo402857r
CrossRef
 
chiral
racemic
Notes:


Polyketides
Phomolide G
C12H20O5 = 244
Synlett    2014, 25 , 501
B. V. S. Reddy, P. S. Reddy, B. P. Reddy, J. S. Yadav
DOI: 10.1055/s-0033-1340348
CrossRef
 
chiral
racemic
Notes:


Polyketides
Phomolide H
C13H22O5 = 258
Synlett    2014, 25 , 501
B. V. S. Reddy, P. S. Reddy, B. P. Reddy, J. S. Yadav
DOI: 10.1055/s-0033-1340348
CrossRef
 
chiral
racemic
Notes:


Polyketides
Berkeleyamide D
C18H21NO5 = 331
Org. Lett.    2014, 16 , 1386
K. Komori, T. Taniguchi, S. Mizutani, K. Monde, K. Kuramochi, K. Tsubaki
DOI: 10.1021/ol500148g
CrossRef
 
chiral
racemic
Notes:


Polyketides
Panclicin-D
C25H45NO5 = 439
Tetrahedron Lett.    2014, 55 , 1952
J. S. Yadav, S. S. Dachavaram, A. Peddapuram, S. Das
DOI: 10.1016/j.tetlet.2014.02.010
CrossRef
 
chiral
racemic
Notes:


Polyketides
Luminacin D
C24H34O8 = 450
Chem. Eur. J.    2014, 20 , 3306
N. Bartlett, L. Gross, F. Péron D. J. Asby, M. D. Selby, A. Tavassoli, B. Linclau
DOI: 10.1002/chem.201304776
CrossRef
 
chiral
racemic
Notes:


Polyketides
Leiodermatolide
C34H51NO8 = 601
Angew. Chem. Int. Ed.    2014, 53 , 2692
I. Paterson, K. K.-H. Ng, S. Williams, D. C. Millican, S. M. Dalby
DOI: 10.1002/anie.201310164
CrossRef
 
chiral
racemic
Notes:


Aromatics
Pulchral
C17H16O3 = 268
Eur. J. Org. Chem.    2014, , 1594
D. Killander, O. Sterner
DOI: 10.1002/ejoc.201301792
CrossRef
 
chiral
racemic
Notes:


Aromatics
Pulchrol
C17H18O3 = 270
Eur. J. Org. Chem.    2014, , 1594
D. Killander, O. Sterner
DOI: 10.1002/ejoc.201301792
CrossRef
 
chiral
racemic
Notes:


Aromatics
Frondosin B
C20H24O2 = 296
J. Am. Chem. Soc.    2014, 136 , 4309
E. Z. Oblak, M. D. VanHeyst, J. Li, A. J. Wiemer, D. L. Wright
DOI: 10.1021/ja413106t
CrossRef
 
chiral
racemic
Notes: synthesis of both enantiomers


Aromatics
Glyceollin I
C20H18O5 = 338
Tetrahedron Lett.    2014, 55 , 1826
Y. Kohno, M. Koso, M. Kuse, H. Takikawa
DOI: 10.1016/j.tetlet.2014.01.142
CrossRef
 
chiral
racemic
Notes: formal synthesis


Aromatics
Rhoiptelol B
C20H24O6 = 360
Synlett    2014, 25 , 661
J. S. Yadav, M. A. Rahman, N. M. Reddy, A. R. Prasad, A. A. K. A. Ghamdi
DOI: 10.1055/s-0033-1340181
CrossRef
 
chiral
racemic
Notes:


Aromatics
Aspercyclide C
C23H26O5 = 382
Chemistry Lett.    2014, 43 , 349
T. Yoshino, S. Yamashita, I. Sato, Y. Hayashi, M. Hirama
DOI: 10.1246/cl.131045
CrossRef
 
chiral
racemic
Notes:


Aromatics
Kopeolone
C24H30O5 = 398
J. Org. Chem.    2014, 79 , 2268
S. Miquet, P. Brémond, B. Ayela, S. R. A. Marque, G. Audran
DOI: 10.1021/jo402572b
CrossRef
 
chiral
racemic
Notes:


Aromatics
Kopeolin
C24H32O5 = 400
J. Org. Chem.    2014, 79 , 2268
S. Miquet, P. Brémond, B. Ayela, S. R. A. Marque, G. Audran
DOI: 10.1021/jo402572b
CrossRef
 
chiral
racemic
Notes:


Aromatics
Podophyllotoxin
C22H22O8 = 414
Angew. Chem. Int. Ed.    2014, 53 , 3115
C. P. Ting, T. J. Maimone
DOI: 10.1002/anie.201311112
CrossRef
 
chiral
racemic
Notes:


Aromatics
Secalonic Acid A
C32H30O13 = 622
Angew. Chem. Int. Ed.    2014, 53 , 3107
T. Qin, J. A. Porco Jr.
DOI: 10.1002/anie.201311260
CrossRef
 
chiral
racemic
Notes:


Aromatics
Secalonic Acid D
C32H30O13 = 622
Angew. Chem. Int. Ed.    2014, 53 , 3107
T. Qin, J. A. Porco Jr.
DOI: 10.1002/anie.201311260
CrossRef
 
chiral
racemic
Notes:


Aromatics
Caraphenol A
C42H28O9 = 676
Angew. Chem. Int. Ed.    2014, 53 , 3409
N. E. Wright, S. A. Snyder
DOI: 10.1002/anie.201311299
CrossRef
 
chiral
racemic
Notes:


Alkaloids
DMDP, 6-Deoxy-
C6H13NO3 = 147
Tetrahedron    2014, 70 , 1880
P. Szcześniak, S. Stecko, O. Staszewska-Krajewska, B. Furman
DOI: 10.1016/j.tet.2014.01.039
CrossRef
 
chiral
racemic
Notes:


Alkaloids
Lentiginosine
C8H15NO2 = 157
Eur. J. Org. Chem.    2014, , 1708
S. Du-a-man, D. Soorukram, C. Kuhakarn, P. Tuchinda, V. Reutrakul, M. Pohmakotr
DOI: 10.1002/ejoc.201301671
CrossRef
 
chiral
racemic
Notes:


Alkaloids
Haliclorensin
C13H28N2 = 212
J. Org. Chem.    2014, 79 , 2792
M. Amat, G. Guignard, N. Llor, J. Bosch
DOI: 10.1021/jo5002627
CrossRef
 
chiral
racemic
Notes:


Alkaloids
Radicamine B
C11H15NO4 = 225
Tetrahedron    2014, 70 , 1880
P. Szcześniak, S. Stecko, O. Staszewska-Krajewska, B. Furman
DOI: 10.1016/j.tet.2014.01.039
CrossRef
 
chiral
racemic
Notes:


Alkaloids
Sedamine, 5-Hydroxy-
C14H21NO2 = 235
Tetrahedron    2014, 70 , 2134
R. W. Bates, N. F. bte M. Aslam, C. H. Tang, O. Simon
DOI: 10.1016/j.tet.2014.02.001
CrossRef
 
chiral
racemic
Notes:


Alkaloids
Funebral
C12H15NO4 = 237
Eur. J. Org. Chem.    2014, , 1431
T.-Y. Yuen, S. E. Eaton, T. M. Woods, D. P. Furkert, K. W. Choi, M. A. Brimble
DOI: 10.1002/ejoc.201301639
CrossRef
 
chiral
racemic
Notes:


Alkaloids
Haliclorensin C
C16H33N = 239
J. Org. Chem.    2014, 79 , 2792
M. Amat, G. Guignard, N. Llor, J. Bosch
DOI: 10.1021/jo5002627
CrossRef
 
chiral
racemic
Notes:


Alkaloids
Pumiliotoxin 251D
C16H29NO = 251
Heterocycles    2014, 89 , 679
S.-S. P. Chou, K.-S. Yang, T.-H. Chiu
DOI: 10.3987/COM-14-12930
CrossRef
 
chiral
racemic
Notes: formal synthesis


Alkaloids
Pinolinone
C15H19NO3 = 261
Chem. Commun.    2014, 50 , 3353
F. Mayr, C. Wiegand, T. Bach
DOI: 10.1039/c3cc49469a
CrossRef
 
chiral
racemic
Notes:


Alkaloids
Physovenine
C14H18N2O3 = 262
Org. Lett.    2014, 16 , 1322
B. Zhou, W. Hou, Y. Yang, H. Feng, Y. Li
DOI: 10.1021/ol500033w
CrossRef
 
chiral
racemic
Notes: formal synthesis


Alkaloids
Lobechine
C14H21NO4 = 267
Eur. J. Org. Chem.    2014, , 1431
T.-Y. Yuen, S. E. Eaton, T. M. Woods, D. P. Furkert, K. W. Choi, M. A. Brimble
DOI: 10.1002/ejoc.201301639
CrossRef
 
chiral
racemic
Notes:


  63 data found. 1 - 30 listed Next Last   
   
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