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Heterocycles Database
Total Synthesis of
Heterocyclic
Natural Products |
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| 1975-2013 |
| 19,943 Compounds |
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27 April, 2012 |
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Search by:
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Carbon:
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Molecular Fomula:
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Molecular Weight:
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Author:
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Journal:
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| Nomenclature : |
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| The natural products are listed under the name used in the original literature. |
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| Journals : |
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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. |
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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 |
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| Editor : |
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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
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| New Total Synthesis of Heterocyclic Natural Products |
| This journal will list natural products with heterocyclic ring
system whose total synthesis has been reported. |
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| 27 April, 2012 |
| | | Search by Journal : | Vol. | No. | | 50 | 37-40 | | 47 | 35, 36 | | 2011 | 25, 26 | | 74 | 9 | | 76 | 17 | | 9 | 18 | | 13 | 17, 18 | | 2011 | 14, 15 | | 2011 | 17, 18 | | 67 | 35, 36, 38, 39 | | 52 | 36-38 | | | |
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| Polyketides |
| Rengyolone |
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C8H10O3 = 154
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Org. Lett.
2012, 14 , 4537
P. D. Brown, A. C. Willis,
M. S. Sherburn, A. L. Lawrence
DOI: 10.1021/ol302042u
CrossRef |
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| chiral |
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| racemic |
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| Notes: |
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| Polyketides |
| Rengyolone |
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C8H10O3 = 154
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Org. Lett.
2012, 14 , 4878
K. Zhao, G.-J. Cheng, H. Yang,
H. Shang, X. Zhang, Y.-D. Wu,
Y. Tang
DOI: 10.1021/ol302205w
CrossRef |
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| chiral |
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| racemic |
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| Notes: |
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| Polyketides |
| Nectriapyrone |
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C11H14O3 = 194
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Tetrahedron
2012, 68 , 7280
O. Geiseler, J. Podlech
DOI: 10.1016/j.tet.2012.06.104
CrossRef |
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| chiral |
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| racemic |
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| Notes: |
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| Polyketides |
| Trochliophorolide B |
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C12H14O3 = 206
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Org. Lett.
2012, 14 , 4698
B. M. Trost, A. Quintard
DOI: 10.1021/ol302074h
CrossRef |
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| chiral |
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| racemic |
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| Notes: |
total synthesis of the proposed structure |
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| Polyketides |
| Xylarone, 8,9-Dehydro- |
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C12H14O3 = 206
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Tetrahedron
2012, 68 , 7280
O. Geiseler, J. Podlech
DOI: 10.1016/j.tet.2012.06.104
CrossRef |
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| chiral |
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| racemic |
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| Notes: |
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| Polyketides |
| Aplysiopsene A |
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C12H16O3 = 208
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Tetrahedron
2012, 68 , 7280
O. Geiseler, J. Podlech
DOI: 10.1016/j.tet.2012.06.104
CrossRef |
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| chiral |
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| racemic |
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| Notes: |
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| Polyketides |
| Helicascolide C |
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C12H18O3 = 210
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Tetrahedron Lett.
2012, 53 , 4997
P. R. Krishna, V. S. Mallula,
P. V. A. Kumar
DOI: 10.1016/j.tetlet.2012.07.018
CrossRef |
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| chiral |
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| racemic |
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| Notes: |
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| Polyketides |
| Umuravumbolide, Deacetyl- |
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C12H18O3 = 210
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Helv. Chim. Acta
2012, 95 , 1593
V. Shekhar, D. K. Reddy,
Y. Venkateswarlu
DOI: 10.1002/hlca.201200078
CrossRef |
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| chiral |
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| racemic |
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| Notes: |
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| Polyketides |
| Helicascolide A |
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C12H20O3 = 212
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Tetrahedron Lett.
2012, 53 , 4997
P. R. Krishna, V. S. Mallula,
P. V. A. Kumar
DOI: 10.1016/j.tetlet.2012.07.018
CrossRef |
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| chiral |
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| racemic |
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| Notes: |
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| Polyketides |
| Patulolide C |
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C12H20O3 = 212
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Org. Biomol. Chem.
2012, 10 , 6995
E. K. Hoegenauer, E. J. Thomas
DOI: 10.1039/c2ob25992c
CrossRef |
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| chiral |
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| racemic |
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| Notes: |
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| Polyketides |
| Patulolide C, epi- |
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C12H20O3 = 212
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Org. Biomol. Chem.
2012, 10 , 6995
E. K. Hoegenauer, E. J. Thomas
DOI: 10.1039/c2ob25992c
CrossRef |
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| chiral |
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| racemic |
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| Notes: |
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| Polyketides |
| Aplysiopsene B |
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C13H18O3 = 222
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Tetrahedron
2012, 68 , 7280
O. Geiseler, J. Podlech
DOI: 10.1016/j.tet.2012.06.104
CrossRef |
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| chiral |
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| racemic |
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| Notes: |
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| Polyketides |
| Aplysiopsene C |
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C13H18O3 = 222
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Tetrahedron
2012, 68 , 7280
O. Geiseler, J. Podlech
DOI: 10.1016/j.tet.2012.06.104
CrossRef |
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| chiral |
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| racemic |
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| Notes: |
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| Polyketides |
| Mycosporulone |
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C11H10O5 = 222
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Org. Lett.
2012, 14 , 4898
M. E. Jung, J. J. Chang
DOI: 10.1021/ol302234a
CrossRef |
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| chiral |
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| racemic |
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| Notes: |
total synthesis of the proposed structure |
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| Polyketides |
| Phomapyrone D |
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C12H14O4 = 222
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Tetrahedron
2012, 68 , 7280
O. Geiseler, J. Podlech
DOI: 10.1016/j.tet.2012.06.104
CrossRef |
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| chiral |
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| racemic |
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| Notes: |
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| Polyketides |
| Phomapyrone A |
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C14H18O3 = 234
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Tetrahedron
2012, 68 , 7280
O. Geiseler, J. Podlech
DOI: 10.1016/j.tet.2012.06.104
CrossRef |
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| chiral |
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| racemic |
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| Notes: |
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| Polyketides |
| Aplysiopsene D |
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C14H20O3 = 236
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Tetrahedron
2012, 68 , 7280
O. Geiseler, J. Podlech
DOI: 10.1016/j.tet.2012.06.104
CrossRef |
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| chiral |
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| racemic |
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| Notes: |
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| Polyketides |
| Umuravumbolide |
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C14H20O4 = 252
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Helv. Chim. Acta
2012, 95 , 1593
V. Shekhar, D. K. Reddy,
Y. Venkateswarlu
DOI: 10.1002/hlca.201200078
CrossRef |
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| chiral |
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| racemic |
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| Notes: |
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| Polyketides |
| Infectopyrone |
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C14H16O5 = 264
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Tetrahedron
2012, 68 , 7280
O. Geiseler, J. Podlech
DOI: 10.1016/j.tet.2012.06.104
CrossRef |
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| chiral |
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| racemic |
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| Notes: |
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| Polyketides |
| Cryptocaryanone A |
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C17H14O4 = 282
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Synlett
2012, 23 , 2129
B. Zhang, Z. Yang, G. Zhao,
B. Ma, X. Xie, X. She
DOI: 10.1055/s-0032-1316580
CrossRef |
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| chiral |
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| racemic |
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| Notes: |
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| Polyketides |
| Phomopsolide B |
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C15H20O6 = 296
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Tetrahedron
2012, 68 , 7489
K. R. Prasad, P. Gutala
DOI: 10.1016/j.tet.2012.06.002
CrossRef |
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| chiral |
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| racemic |
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| Notes: |
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| Polyketides |
| Incarviditone |
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C16H20O6 = 308
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Org. Lett.
2012, 14 , 4537
P. D. Brown, A. C. Willis,
M. S. Sherburn, A. L. Lawrence
DOI: 10.1021/ol302042u
CrossRef |
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| chiral |
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| racemic |
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| Notes: |
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| Polyketides |
| Incarviditone |
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C16H20O6 = 308
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Org. Lett.
2012, 14 , 4878
K. Zhao, G.-J. Cheng, H. Yang,
H. Shang, X. Zhang, Y.-D. Wu,
Y. Tang
DOI: 10.1021/ol302205w
CrossRef |
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| chiral |
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| racemic |
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| Notes: |
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| Polyketides |
| Incarvilleatone |
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C16H20O6 = 308
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Org. Lett.
2012, 14 , 4537
P. D. Brown, A. C. Willis,
M. S. Sherburn, A. L. Lawrence
DOI: 10.1021/ol302042u
CrossRef |
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| chiral |
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| racemic |
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| Notes: |
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| Polyketides |
| Incarvilleatone |
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C16H20O6 = 308
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Org. Lett.
2012, 14 , 4878
K. Zhao, G.-J. Cheng, H. Yang,
H. Shang, X. Zhang, Y.-D. Wu,
Y. Tang
DOI: 10.1021/ol302205w
CrossRef |
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| chiral |
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| racemic |
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| Notes: |
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| Polyketides |
| Seimatopolide A |
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C18H32O5 = 328
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Eur. J. Org. Chem.
2012, , 4910
C. R. Reddy, N. N. Rao,
M. D. Reddy
DOI: 10.1002/ejoc.201200732
CrossRef |
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| chiral |
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| racemic |
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| Notes: |
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| Polyketides |
| Sch 725680 |
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C21H22O7 = 386
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Org. Lett.
2012, 14 , 4303
T. Takeuchi, Y. Mizushina,
S. Takaichi, N. Inoue,
K. Kuramochi, S. Shimura,
Y. Myobatake, Y. Katayama,
K. Takemoto, S. Endo,
S. Kamisuki, F. Sugawara
DOI: 10.1021/ol301865u
CrossRef |
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| chiral |
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| racemic |
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| Notes: |
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| Polyketides |
| Aureothin |
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C22H23NO6 = 397
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Angew. Chem. Int. Ed.
2012, 51 , 9587
M. Henrot, M. E. A. Richter,
J. Maddaluno, C. Hertweck,
Michaël De Paolis
DOI: 10.1002/anie.201204259
CrossRef |
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| chiral |
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| racemic |
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| Notes: |
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| Polyketides |
| Ripostatin A |
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C30H38O6 = 494
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Org. Lett.
2012, 14 , 4690
W. Tang, E. V. Prusov
DOI: 10.1021/ol302219x
CrossRef |
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| chiral |
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| racemic |
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| Notes: |
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| Polyketides |
| Dictyostatin |
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C32H52O6 = 532
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Chem. Eur. J.
2012, 18 , 11788
J. Gallon, J. Esteban,
S. Bouzbouz, M. Campbell,
S. Reymond, J. Cossy
DOI: 10.1002/chem.201201001
CrossRef |
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| chiral |
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| racemic |
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| Notes: |
formal synthesis |
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