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.

57 data found. 1 - 30 listed Next Last
Polyketides

Parvistone C

C14H16O4 = 248
J. Heterocycl. Chem. 2019, 56, 815
R. R. Addada, V. R. Regalla, S. R. G. Venkata, V. N. Vema, V. R. Anna
DOI: 10.1093/ejcts/ezz109
CrossRef
chiral
racemic
Notes:
Polyketides

Penicillinolide A

C14H24O5 = 272
Synthesis 2019, 51, 1427
M. S. Reddy, G. Manikanta, P. R. Krishna
DOI: 10.1055/s-0037-1611040
CrossRef
chiral
racemic
Notes:
Polyketides

Vermiculine

C20H24O8 = 392
Chem. Eur. J. 2019, 25, 3532
P. Steib, B. Breit
DOI: 10.1002/chem.201900216
CrossRef
chiral
racemic
Notes:
Aromatics

Cladosporin

C16H20O5 = 292
Tetrahedron Lett. 2019, 60, 831
P. Das, Y. Mankad, D. S. Reddy
DOI: 10.1016/j.tetlet.2019.02.012
CrossRef
chiral
racemic
Notes:
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:
Aromatics

Salimabromide

C20H20O3Br2 = 468
Org. Lett. 2019, 21, 1939
A. Palm, C. Knopf, B. Schmalzbauer, D. Menche
DOI: 10.1021/acs.orglett.9b00706
CrossRef
chiral
racemic
Notes:
Aromatics

Chalcitrin

C35H22O15 = 682
J. Am. Chem. Soc. 2019, 141, 4515
M. Yang, F. Yin, H. Fujino, S. A. Snyder
DOI: 10.1021/jacs.8b12612
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:
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:
Steroids

Pennogenin

C27H42O4 = 430
Tetrahedron 2019, 75, 1717
R. Gao, Y. Shi, W.-S. Tian
DOI: 10.1016/j.tet.2018.11.009
CrossRef
chiral
racemic
Notes:
Alkaloids

Actinidine

C10H13N = 147
Chem. Commun. 2019, 55, 3270
D. Uredi, D. R. Motati, E. B. Watkins 
DOI: 10.1039/C9CC01097A
CrossRef
chiral
racemic
Notes:
Alkaloids

Leuvalin

C11H18N2O = 194
J. Org. Chem. 2019, 84, 3647
R. Ramesh, M. T. Bovino, Y. Zeng, J. Aubé
DOI: 10.1021/acs.joc.8b03206
CrossRef
chiral
racemic
Notes:
Alkaloids

Chimonamidine

C12H16N2O2 = 220
Angew. Chem. Int. Ed. 2019, 58, 3402
M. Moskowitz, C. Wolf
DOI: 10.1002/anie.201981713
CrossRef
chiral
racemic
Notes:
Alkaloids

Phevalin

C14H16N2O = 228
J. Org. Chem. 2019, 84, 3647
R. Ramesh, M. T. Bovino, Y. Zeng, J. Aubé
DOI: 10.1021/acs.joc.8b03206
CrossRef
chiral
racemic
Notes:
Alkaloids

Phileucin

C15H18N2O = 242
J. Org. Chem. 2019, 84, 3647
R. Ramesh, M. T. Bovino, Y. Zeng, J. Aubé
DOI: 10.1021/acs.joc.8b03206
CrossRef
chiral
racemic
Notes:
Alkaloids

Tyrvalin

C14H16N2O2 = 244
J. Org. Chem. 2019, 84, 3647
R. Ramesh, M. T. Bovino, Y. Zeng, J. Aubé
DOI: 10.1021/acs.joc.8b03206
CrossRef
chiral
racemic
Notes:
Alkaloids

Mersicarpine

C17H20N2O2 = 284
Chem. Commun. 2019, 55, 3544
Y. Liua, H. Wang
DOI: 10.1039/C8CC09949A
CrossRef
chiral
racemic
Notes:
Alkaloids

Morphine

C17H19NO3 = 285
Org. Lett. 2019, 21, 1347
J. Brousseau, A. Xolin, L. Barriault
DOI: 10.1021/acs.orglett.9b00044
CrossRef
chiral
racemic
Notes: formal synthesis
Alkaloids

Gephyrotoxin

C19H29NO = 287
Angew. Chem. Int. Ed. 2019, 58, 3809
Y. Chen, Y.-M. He, S. Zhang, T. Miao, Q.-H. Fan
DOI: 10.1002/anie.201981713
CrossRef
chiral
racemic
Notes: formal synthesis
Alkaloids

Cylindricine C

C19H33NO2 = 307
Angew. Chem. Int. Ed. 2019, 58, 4381
S. Hiraoka, T. Matsumoto, K. Matsuzaka, T. Sato, N. Chida
DOI: 10.1002/anie.201981713
CrossRef
chiral
racemic
Notes:
Alkaloids

Melodinine E

C19H20N2O2 = 308
Chem. Commun. 2019, 55, 3544
Y. Liua, H. Wang
DOI: 10.1039/C8CC09949A
CrossRef
chiral
racemic
Notes:
Alkaloids

Vincamone, 19-OH-∆14-

C19H20N2O2 = 308
J. Am. Chem. Soc. 2019, 141, 4811
B. M. Trost, Y. Bai, W.-J. Bai, J. E. Schultz
DOI: 10.1021/jacs.9b00788
CrossRef
chiral
racemic
Notes:
Alkaloids

Eburnamine, 19-Oxo-

C19H22N2O2 = 310
J. Am. Chem. Soc. 2019, 141, 4811
B. M. Trost, Y. Bai, W.-J. Bai, J. E. Schultz
DOI: 10.1021/jacs.9b00788
CrossRef
chiral
racemic
Notes:
57 data found. 1 - 30 listed Next Last