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. 31 - 57 listedFirst Previous
Alkaloids

Eburnamonine, 19-OH-

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:
Alkaloids

Leuconoxine

C19H22N2O2 = 310
Chem. Commun. 2019, 55, 3544
Y. Liua, H. Wang
DOI: 10.1039/C8CC09949A
CrossRef
chiral
racemic
Notes:
Alkaloids

Eburnamine, 19-OH-

C19H24N2O2 = 312
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

Spectalin

C20H39NO2 = 325
Chem. Pharm. Bull. 2019, 67, 253
R. Kameda, T. Sohma, K. Kobayashi, R. Uchiyama, K. Nosaka, H. Konno, K. Akaji, Y. Hattori
DOI: 10.1248/cpb.c18-00817
CrossRef
chiral
racemic
Notes:
Alkaloids

Spectalin, Iso-6-

C20H39NO2 = 325
Chem. Pharm. Bull. 2019, 67, 253
R. Kameda, T. Sohma, K. Kobayashi, R. Uchiyama, K. Nosaka, H. Konno, K. Akaji, Y. Hattori
DOI: 10.1248/cpb.c18-00817
CrossRef
chiral
racemic
Notes:
Alkaloids

Scholarisine G

C19H22N2O3 = 326
Chem. Commun. 2019, 55, 3544
Y. Liua, H. Wang
DOI: 10.1039/C8CC09949A
CrossRef
chiral
racemic
Notes:
Alkaloids

Fasicularin

C20H34N2S = 334
Org. Lett. 2019, 21, 1868
S. Yamamoto, Y. Komiya, A. Kobayashi, R. Minamikawa, T. Oishi, T. Sato, N. Chida
DOI: 10.1021/acs.orglett.9b00478
CrossRef
chiral
racemic
Notes:
Alkaloids

Chilenamine

C20H21NO4 = 339
J. Org. Chem. 2019, 84, 2870
W. Zhu, S. Tong, J. Zhu, M.-X. Wang
DOI: 10.1002/ejoc.201900640
CrossRef
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

Ambiguine P

C25H29NO = 359
J. Am. Chem. Soc. 2019, 141, 4820
J.Xu, V. H. Rawal
DOI: 10.1021/jacs.9b01739
CrossRef
chiral
racemic
Notes:
Alkaloids

Isodesmopyridine

C18H28N4O6 = 396
Tetrahedron Lett. 2019, 60, 928
W. Fuse, A. Imura, N. Tanaka, T. Usuki
DOI: 10.1016/j.tetlet.2019.02.038
CrossRef
chiral
racemic
Notes:
Alkaloids

Palmanine

C21H21NO7 = 399
J. Org. Chem. 2019, 84, 2870
W. Zhu, S. Tong, J. Zhu, M.-X. Wang
DOI: 10.1002/ejoc.201900640
CrossRef
chiral
racemic
Notes:
Alkaloids

Madangamine C

C28H44N2 = 408
Bull. Chem. Soc. Japan 2019, 92, 545
T. Suto,Y. Yanagita, Y. Nagashima, S. Takikawa, Y. Kurosu, N. Matsuo, K. Miura, S. Simizu, T. Sato, N. Chida
DOI: 10.1246/bcsj.20180334
CrossRef
chiral
racemic
Notes:
Alkaloids

Madangamine E

C28H46N2 = 410
Bull. Chem. Soc. Japan 2019, 92, 545
T. Suto,Y. Yanagita, Y. Nagashima, S. Takikawa, Y. Kurosu, N. Matsuo, K. Miura, S. Simizu, T. Sato, N. Chida
DOI: 10.1246/bcsj.20180334
CrossRef
chiral
racemic
Notes:
Alkaloids

Anibamine

C30H50N = 424
Org. Biomol. Chem. 2019, 17, 2896
T. Miyakoshi, H. Konno 
DOI: 10.1039/C8OB02723D
CrossRef
chiral
racemic
Notes: TFAsalt
Alkaloids

Madangamine D

C29H48N2 = 424
Bull. Chem. Soc. Japan 2019, 92, 545
T. Suto,Y. Yanagita, Y. Nagashima, S. Takikawa, Y. Kurosu, N. Matsuo, K. Miura, S. Simizu, T. Sato, N. Chida
DOI: 10.1246/bcsj.20180334
CrossRef
chiral
racemic
Notes:
Alkaloids

Madangamine A

C30H44N2 = 432
Bull. Chem. Soc. Japan 2019, 92, 545
T. Suto,Y. Yanagita, Y. Nagashima, S. Takikawa, Y. Kurosu, N. Matsuo, K. Miura, S. Simizu, T. Sato, N. Chida
DOI: 10.1246/bcsj.20180334
CrossRef
chiral
racemic
Notes:
Alkaloids

Madangamine B

C30H44N2 = 432
J. Am. Chem. Soc. 2019, 92, 545
T. Suto,Y. Yanagita, Y. Nagashima, S. Takikawa, Y. Kurosu, N. Matsuo, K. Miura, S. Simizu, T. Sato, N. Chida
DOI: 10.1246/bcsj.20180334
CrossRef
chiral
racemic
Notes:
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

Et-743

C39H43N3O11S = 761
Angew. Chem. Int. Ed. 2019, 58, 3972
W. He, Z. Zhang, D. Ma
DOI: 10.1002/anie.201981713
CrossRef
chiral
racemic
Notes:
Alkaloids

Lurbinectedin

C41H44N4O10S = 784
Angew. Chem. Int. Ed. 2019, 58, 3972
W. He, Z. Zhang, D. Ma
DOI: 10.1002/anie.201981713
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

Melearoride A

C30H47NO4 = 485
Tetrahedron Lett. 2019, 60, 743
C. W. Reed, M. G. Fulton, K. D. Nance, C. W. Lindsley
DOI: 10.1016/j.tetlet.2019.02.006
CrossRef
chiral
racemic
Notes:
Miscellaneous

Doliclide

C27H41IN2O6 = 616
Helv. Chim. Acta 2019, 102, e1900023
W. Che, D. C. Wen, S.-F. Zhu, Q.-L. Zhou
DOI: 10.1002/hlca.201900023
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:
Miscellaneous

Mozamide A

C45H64N8O8 = 844
J. Org. Chem. 2019, 84, 2489
L. Junk, U. Kazamaier
DOI: 10.1021/acs.joc.8b02836
CrossRef
chiral
racemic
Notes:
57 data found. 31 - 57 listedFirst Previous