Heterocycles Database
Total Synthesis of
Heterocyclic
Natural Products
 
 1975-2014
 19,943 Compounds
 27 April, 2012
 
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Group

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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
  85 data found. 1 - 30 listed Next Last   

Polyketides
cis-Whisky Lactone
C9H16o2 = 156
J. Org. Chem.    2014, 79 , 976
J. Swatschek, L. Grothues, J. O. Bauer, C. Strohmann, M. Christmann
DOI: 10.1021/jo402422b
CrossRef
 
chiral
racemic
Notes:


Polyketides
cis-Cognac Lactone
C10H18O2 = 170
J. Org. Chem.    2014, 79 , 976
J. Swatschek, L. Grothues, J. O. Bauer, C. Strohmann, M. Christmann
DOI: 10.1021/jo402422b
CrossRef
 
chiral
racemic
Notes:


Polyketides
Aerangis Lactone, cis-
C11H20O2 = 184
J. Org. Chem.    2014, 79 , 976
J. Swatschek, L. Grothues, J. O. Bauer, C. Strohmann, M. Christmann
DOI: 10.1021/jo402422b
CrossRef
 
chiral
racemic
Notes:


Polyketides
Decarestrictine D
C10H16O5 = 216
Tetrahedron Asymmetry    2014, 25 , 203
K. Vamshikrishna, G. Srinu, P. Srihari
DOI: 10.1016/j.tetasy.2013.12.008
CrossRef
 
chiral
racemic
Notes:


Polyketides
Decarestrictine O
C10H16O5 = 216
Tetrahedron Asymmetry    2014, 25 , 203
K. Vamshikrishna, G. Srinu, P. Srihari
DOI: 10.1016/j.tetasy.2013.12.008
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
Cytospolide D
C15H26O4 = 270
Eur. J. Org. Chem.    2014, , 860
R. K. Rej, S. Nanda
DOI: 10.1002/ejoc.201301365
CrossRef
 
chiral
racemic
Notes:


Polyketides
Cytospolide E
C15H26O4 = 270
Eur. J. Org. Chem.    2014, , 860
R. K. Rej, S. Nanda
DOI: 10.1002/ejoc.201301365
CrossRef
 
chiral
racemic
Notes:


Polyketides
Seimatopolide A
C18H32O5 = 328
J. Org. Chem.    2014, 79 , 1461
K. R. Prasad, O. Revu
DOI: 10.1021/jo4023827
CrossRef
 
chiral
racemic
Notes: synthesis of enantiomer


Polyketides
Seimatopolide A
C18H32O5 = 328
Tetrahedron Asymmetry    2013, 24 , 1576
N. Kavitha, V. P. Kumar, C. S. Reddy, S. Chandrasekhar
DOI: 10.1016/j.tetasy.2013.10.010
CrossRef
 
chiral
racemic
Notes:


Polyketides
Lippialactone
C18H24O8 = 368
Synthesis    2014, 46 , 307
P. R. Krishna, R. Nomula, R. Kunde
DOI: 10.1055/s-0033-1340314
CrossRef
 
chiral
racemic
Notes:


Polyketides
Boronolide
C18H26O8 = 370
Tetrahedron Lett.    2014, 55 , 1398
B. V. S. Reddy, V. V. Reddy, K. Praneeth
DOI: 10.1016/j.tetlet.2013.12.061
CrossRef
 
chiral
racemic
Notes:


Polyketides
Anamarine
C20H26O10 = 426
Tetrahedron Lett.    2014, 55 , 1398
B. V. S. Reddy, V. V. Reddy, K. Praneeth
DOI: 10.1016/j.tetlet.2013.12.061
CrossRef
 
chiral
racemic
Notes:


Polyketides
Spicigerolide, 8-epi-
C20H26O10 = 426
Tetrahedron Lett.    2014, 55 , 1398
B. V. S. Reddy, V. V. Reddy, K. Praneeth
DOI: 10.1016/j.tetlet.2013.12.061
CrossRef
 
chiral
racemic
Notes:


Polyketides
Carolacton
C25H40O8 = 468
Org. Lett.    2014, 16 , 1148
M. S. Hallside, R. S. Brzozowski, W. M. Wuest, A. J. Phillips
DOI: 10.1021/ol500004k
CrossRef
 
chiral
racemic
Notes:


Polyketides
Pladienolide B
C30H48O8 = 536
Eur. J. Org. Chem.    2014, , 1025
S. Müller, F. Sasse, M. E. Maier
DOI: 10.1002/ejoc.201301468
CrossRef
 
chiral
racemic
Notes:


Polyketides
Didemnaketal B
C52H86O15 = 950
Chem. Eur. J.    2014, 20 , 1848
H. Fuwa, T. Muto, K. Sekine, M. Sasaki
DOI: 10.1002/chem.201303713
CrossRef
 
chiral
racemic
Notes: synthesis of revised structure


Aromatics
Phthalide, Butyl-7-hydroxy-
C12H14O3 = 206
Tetrahedron Lett.    2014, 55 , 1303
C. Sreelakshmi, A. B. Rao, M. L. Narasu, P. J. Reddy, B. V. S. Reddy
DOI: 10.1016/j.tetlet.2013.12.089
CrossRef
 
chiral
racemic
Notes:


Aromatics
No Name
C16H14O3 = 254
Synthesis    2014, 46 , 465
S. V. N. Vuppalapati, L. Xia, N. Edayadulla, Y. R. Lee
DOI: 10.1055/s-0033-1340466
CrossRef
 
chiral
racemic
Notes:


Aromatics
Paecilocin A
C16H22O3 = 262
Tetrahedron Lett.    2014, 55 , 1303
C. Sreelakshmi, A. B. Rao, M. L. Narasu, P. J. Reddy, B. V. S. Reddy
DOI: 10.1016/j.tetlet.2013.12.089
CrossRef
 
chiral
racemic
Notes:


Aromatics
Thysanone
C14H12O6 = 276
Synlett    2014, 25 , 556
K. Schünemann, D. P. Furkert, S. Connelly, J. D. Fraser, J. Sperry, M. A. Brimble
DOI: 10.1055/s-0033-1340495
CrossRef
 
chiral
racemic
Notes:


Aromatics
No Name
C17H16O4 = 284
Synthesis    2014, 46 , 465
S. V. N. Vuppalapati, L. Xia, N. Edayadulla, Y. R. Lee
DOI: 10.1055/s-0033-1340466
CrossRef
 
chiral
racemic
Notes:


Aromatics
No Name
C17H16O4 = 284
Synthesis    2014, 46 , 465
S. V. N. Vuppalapati, L. Xia, N. Edayadulla, Y. R. Lee
DOI: 10.1055/s-0033-1340466
CrossRef
 
chiral
racemic
Notes:


Aromatics
Centrolobine
C20H24O3 = 312
Tetrahedron Asymmetry    2014, 25 , 305
Z. Yang, H.-D. Kim
DOI: 10.1016/j.tetasy.2013.12.019
CrossRef
 
chiral
racemic
Notes:


Aromatics
Americanin A, Iso-
C18H16O6 = 328
Eur. J. Org. Chem.    2014, , 1037
L. I. Pilkington, D. Barker
DOI: 10.1002/ejoc.201301363
CrossRef
 
chiral
racemic
Notes:


Aromatics
Americanol A, Iso-
C18H18O6 = 330
Eur. J. Org. Chem.    2014, , 1037
L. I. Pilkington, D. Barker
DOI: 10.1002/ejoc.201301363
CrossRef
 
chiral
racemic
Notes:


Aromatics
Arizonin B1
C17H14O7 = 330
Tetrahedron Asymmetry    2013, 24 , 1548
R. A. Fernandes, S. V. Mulay, V. P. Chavan
DOI: 10.1016/j.tetasy.2013.10.011
CrossRef
 
chiral
racemic
Notes:


Aromatics
Arizonin C1
C18H16O7 = 344
Tetrahedron Asymmetry    2013, 24 , 1548
R. A. Fernandes, S. V. Mulay, V. P. Chavan
DOI: 10.1016/j.tetasy.2013.10.011
CrossRef
 
chiral
racemic
Notes:


Aromatics
Boletopsin 7
C22H16O9 = 424
J. Org. Chem.    2014, 79 , 1017
A. M. Beekman, R. A. Barrow
DOI: 10.1021/jo402492d
CrossRef
 
chiral
racemic
Notes:


  85 data found. 1 - 30 listed Next Last   
   
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