HETEROCYCLES
An International Journal for Reviews and Communications in Heterocyclic ChemistryWeb Edition ISSN: 1881-0942
Published online by The Japan Institute of Heterocyclic Chemistry
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Natural Products with Heterocyclic Ring System
Synthesis
New Heterocyclic Natural Products
Updated: 20 December, 2019
This journal will list the new natural products with a heterocyclic ring system, collected from current chemical literature, whose synthesis has been established.
- Search by Group: AllPolyketidesAromaticsTerpenesSteroidsAlkaloidsAntibioticsMiscellaneous
- Search by Journal: Angew. Chem. Int. Ed.Bull. Chem. Soc. JapanChem. Commun.Chem. Eur. J.Chem. Pharm. Bull.Helv. Chim. ActaJ. Am. Chem. Soc.J. Heterocycl. Chem.J. Org. Chem.Org. Biomol. Chem.Org. Lett.SynthesisTetrahedronTetrahedron Lett.
- Year: 20192019201920192019201920192019201920192019201920192019
- Vol: 5892552567102141 9256841721517560
- No: 11-13322, 24143311, 12 335, 6115, 661210, 12, 13
9 data found. 1 - 9 listed
Terpenes
Botrydial, 10-Oxodehydrodihydro-
C15H18O2 = 230
Tetrahedron 2019, 75, 1739
C. Qiao, W. Zhang, J.-C. Han,
W.-M. Dai, C.-C. Li
DOI: 10.1016/j.tet.2018.11.019
CrossRef
| chiral |  |
| racemic |  |
| Notes: |
Terpenes
Diendial, 10-Oxodihydrobotry-1(9),4(5)-
C15H20O2 = 232
Tetrahedron 2019, 75, 1739
C. Qiao, W. Zhang, J.-C. Han,
W.-M. Dai, C.-C. Li
DOI: 10.1016/j.tet.2018.11.019
CrossRef
| chiral | |
| racemic | |
| Notes: |
Terpenes
Aplykurodinone-1
C20H30O3 = 318
Tetrahedron Lett. 2019, 60, 839
Y. Peng, Y. Sun, B. Wang,
Y. Zhou, S. Huang, X. Wang
DOI: 10.1016/j.tetlet.2019.02.019
CrossRef
| chiral | |
| racemic | |
| Notes: | formal synthesis |
Terpenes
Rhodomyrtusial A
C30H44O4 = 468
Angew. Chem. Int. Ed. 2019, 58, 4291
X.-J. Qin, T. J. Rauwolf, P.-P. Li,
H. Liu, J. McNeely, Y. Hua,
H.-Y. Liu, J. A. Porco, Jr.
DOI: 10.1002/anie.201981713
CrossRef
| chiral | |
| racemic | |
| Notes: |
Terpenes
Rhodomyrtusial C
C30H44O4 = 468
Angew. Chem. Int. Ed. 2019, 58, 4291
X.-J. Qin, T. J. Rauwolf, P.-P. Li,
H. Liu, J. McNeely, Y. Hua,
H.-Y. Liu, J. A. Porco, Jr.
DOI: 10.1002/anie.201814421
CrossRef
| chiral | |
| racemic | |
| Notes: |
Terpenes
Rhotomentodione A
C30H44O4 = 468
Angew. Chem. Int. Ed. 2019, 58, 4291
X.-J. Qin, T. J. Rauwolf, P.-P. Li,
H. Liu, J. McNeely, Y. Hua,
H.-Y. Liu, J. A. Porco, Jr.
DOI: 10.1002/anie.201814421
CrossRef
| chiral | |
| racemic | |
| Notes: |
Terpenes
Rhotomentodione B
C30H44O4 = 468
Angew. Chem. Int. Ed. 2019, 58, 4291
X.-J. Qin, T. J. Rauwolf, P.-P. Li,
H. Liu, J. McNeely, Y. Hua,
H.-Y. Liu, J. A. Porco, Jr.
DOI: 10.1002/anie.201981713
CrossRef
| chiral | |
| racemic | |
| Notes: |
Terpenes
Tomentodione Q
C30H44O4 = 468
Angew. Chem. Int. Ed. 2019, 58, 4291
X.-J. Qin, T. J. Rauwolf, P.-P. Li,
H. Liu, J. McNeely, Y. Hua,
H.-Y. Liu, J. A. Porco, Jr.
DOI: 10.1002/anie.201981713
CrossRef
| chiral | |
| racemic | |
| Notes: |
Terpenes
Tomentodione R
C30H44O4 = 468
Angew. Chem. Int. Ed. 2019, 58, 4291
X.-J. Qin, T. J. Rauwolf, P.-P. Li,
H. Liu, J. McNeely, Y. Hua,
H.-Y. Liu, J. A. Porco, Jr.
DOI: 10.1002/anie.201981713
CrossRef
| chiral | |
| racemic | |
| Notes: |
9 data found. 1 - 9 listed
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