

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: 58925525671021419256841721517560
- No: 11-13322, 24143311, 12335, 6115, 661210, 12, 13
9 data found. 1 - 9 listed
Aromatics
Hypocrolide A
C26H30O7 = 454
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
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: |
Steroids
Pennogenin
C27H42O4 = 430
chiral | ![]() |
racemic | ![]() |
Notes: |
Alkaloids
Manzacidin A
C12H14N3O4Br = 344
Tetrahedron 2019, 75, 1767
Y. Liu, Z. Ruan, Y. Wang,
S.-H. Huang, R. Hong
DOI: 10.1016/j.tet.2018.12.026
CrossRef
chiral | ![]() |
racemic | ![]() |
Notes: | formal synthesis |
Alkaloids
Manzacidin C
C12H14N3O4Br = 344
Tetrahedron 2019, 75, 1767
Y. Liu, Z. Ruan, Y. Wang,
S.-H. Huang, R. Hong
DOI: 10.1016/j.tet.2018.12.026
CrossRef
chiral | ![]() |
racemic | ![]() |
Notes: | formal synthesis |
Alkaloids
Vindoline
C25H32N2O6 = 456
Tetrahedron 2019, 75, 1751
W. Chen, H. Tian, W. Tan, X. Liu,
X. Yang, H. Zhang
DOI: 10.1016/j.tet.2018.11.046
CrossRef
chiral | ![]() |
racemic | ![]() |
Notes: |
Alkaloids
Cephalostatin 1
C54H74N2O10 = 910
Tetrahedron 2019, 75, 1722
Y. Shi, Q. Xiao, Q. Lan,
D.-H. Wang, L.-Q. Jia, X.-H. Tang,
T. Zhou, M. Li, W.-S. Tian
DOI: 10.1016/j.tet.2018.11.010
CrossRef
chiral | ![]() |
racemic | ![]() |
Notes: |
Miscellaneous
Nannocystin Ax
C42H35N3O8Cl2 = 800
Tetrahedron 2019, 75, 1781
R. Liu, M. Xia, Y. Zhang, S. Fu,
B. Liu
DOI: 10.1016/j.tet.2018.12.021
CrossRef
chiral | ![]() |
racemic | ![]() |
Notes: |
9 data found. 1 - 9 listed