Natural Products with Heterocyclic Ring System

Synthesis

New Heterocyclic Natural Products

Updated: 16 July, 2019

This journal will list the new natural products with a heterocyclic ring system, collected from current chemical literature, whose synthesis has been established.

79 data found. 1 - 30 listed Next Last
Polyketides

Gibepyrone A

C10H12O2 = 164
Eur. J. Org. Chem. 2018, , 3144
I. Burkhardt, J. S. Dickschat
DOI: 10.1002/ejoc.201800621
CrossRef
chiral
racemic
Notes:
Polyketides

No Name

C10H14O2 = 166
Eur. J. Org. Chem. 2018, , 3144
I. Burkhardt, J. S. Dickschat
DOI: 10.1002/ejoc.201800621
CrossRef
chiral
racemic
Notes:
Polyketides

Gibepyrone A, 4-Hydroxy-

C10H12O3 = 180
Eur. J. Org. Chem. 2018, , 3144
I. Burkhardt, J. S. Dickschat
DOI: 10.1002/ejoc.201800621
CrossRef
chiral
racemic
Notes:
Polyketides

Germicidin C

C10H14O3 = 182
Eur. J. Org. Chem. 2018, , 3144
I. Burkhardt, J. S. Dickschat
DOI: 10.1002/ejoc.201800621
CrossRef
chiral
racemic
Notes:
Polyketides

Nectriapyrone

C11H14O3 = 194
Eur. J. Org. Chem. 2018, , 3144
I. Burkhardt, J. S. Dickschat
DOI: 10.1002/ejoc.201800621
CrossRef
chiral
racemic
Notes:
Polyketides

Nonenolide

C10H16O4 = 200
J. Nat. Prod. 2018, 81, 1399
P. R. Sudina, D. R. Motati, A. Seema
DOI: 10.1021/acs.jnatprod.8b00001
CrossRef
chiral
racemic
Notes:
Polyketides

Prolipyrone A

C12H18O3 = 210
Eur. J. Org. Chem. 2018, , 3144
I. Burkhardt, J. S. Dickschat
DOI: 10.1002/ejoc.201800621
CrossRef
chiral
racemic
Notes:
Polyketides

Amphidinolide F

C35H52O9 = 616
Org. Lett. 2018, 20, 3192
L. Ferrié, J. Fenneteau, B. Figadère
DOI: 10.1021/acs.orglett.8b01020
CrossRef
chiral
racemic
Notes:
Aromatics

Conicol

C16H20O2 = 244
Angew. Chem. Int. Ed. 2018, 57, 7654
Y. Sempere, E. M. Carreira
DOI: 10.1002/anie.201885013
CrossRef
chiral
racemic
Notes: formal synthesis
Aromatics

Sakisacaulon A

C23H28O7 = 416
J. Nat. Prod. 2018, 81, 1460
T. K. Kim, J. E. Kim, U. J. Youn, S. J. Han, Il-C. Kim, C.-G. Cho, J. H. Yim
DOI: 10.1021/acs.jnatprod.8b00227
CrossRef
chiral
racemic
Notes:
Aromatics

Lobaric Acid

C24H26O8 = 442
J. Nat. Prod. 2018, 81, 1460
T. K. Kim, J. E. Kim, U. J. Youn, S. J. Han, Il-C. Kim, C.-G. Cho, J. H. Yim
DOI: 10.1021/acs.jnatprod.8b00227
CrossRef
chiral
racemic
Notes:
Aromatics

Lobarstin

C24H26O8 = 442
J. Nat. Prod. 2018, 81, 1460
T. K. Kim, J. E. Kim, U. J. Youn, S. J. Han, Il-C. Kim, C.-G. Cho, J. H. Yim
DOI: 10.1021/acs.jnatprod.8b00227
CrossRef
chiral
racemic
Notes:
Aromatics

Lobarin

C24H28O9 = 460
J. Nat. Prod. 2018, 81, 1460
T. K. Kim, J. E. Kim, U. J. Youn, S. J. Han, Il-C. Kim, C.-G. Cho, J. H. Yim
DOI: 10.1021/acs.jnatprod.8b00227
CrossRef
chiral
racemic
Notes:
Aromatics

Methyllobarin

C25H30O9 = 474
J. Nat. Prod. 2018, 81, 1460
T. K. Kim, J. E. Kim, U. J. Youn, S. J. Han, Il-C. Kim, C.-G. Cho, J. H. Yim
DOI: 10.1021/acs.jnatprod.8b00227
CrossRef
chiral
racemic
Notes:
Aromatics

Psiguadial B

C30H34O5 = 474
J. Org. Chem. 2018, 83, 6066
L. M. Chapman, J. C. Beck, C. R. Lacker, L. Wu, S. E. Reisman
DOI: 10.1021/acs.joc.8b00728
CrossRef
chiral
racemic
Notes:
Aromatics

Boletopsin 11

C26H24O9 = 480
J. Org. Chem. 2018, 83, 6776
M. Y. Zhang, R. A. Barrow
DOI: 10.1021/acs.joc.8b00792
CrossRef
chiral
racemic
Notes:
Aromatics

Phomopsis-H76 A

C30H30O12 = 582
Chem. Eur. J. 2018, 24, 8760
G. Valdomir, S. Senthilkumar, D. Ganapathy, Y. Zhang, L. F. Tietze
DOI: 10.1002/chem.201801323
CrossRef
chiral
racemic
Notes:
Aromatics

Blennolide H

C32H30O14 = 638
Chem. Eur. J. 2018, 24, 8760
G. Valdomir, S. Senthilkumar, D. Ganapathy, Y. Zhang, L. F. Tietze
DOI: 10.1002/chem.201801323
CrossRef
chiral
racemic
Notes:
Terpenes

Boschnialactone, 7-epi-

C9H14O2 = 154
J. Org. Chem. 2018, 83, 6086
H. P. A. Khan, D. Das, T. K. Chakraborty
DOI: 10.1021/acs.joc.8b00752
CrossRef
chiral
racemic
Notes:
Terpenes

Dolicholactone

C10H14O2 = 166
J. Org. Chem. 2018, 83, 6086
H. P. A. Khan, D. Das, T. K. Chakraborty
DOI: 10.1021/acs.joc.8b00752
CrossRef
chiral
racemic
Notes:
Terpenes

Teucriumlactone

C10H14O2 = 166
J. Org. Chem. 2018, 83, 6086
H. P. A. Khan, D. Das, T. K. Chakraborty
DOI: 10.1021/acs.joc.8b00752
CrossRef
chiral
racemic
Notes:
Terpenes

Iridomyrmecin

C10H16O2 = 168
J. Org. Chem. 2018, 83, 6086
H. P. A. Khan, D. Das, T. K. Chakraborty
DOI: 10.1021/acs.joc.8b00752
CrossRef
chiral
racemic
Notes:
Terpenes

Iridomyrmecin, Iso-

C10H16O2 = 168
J. Org. Chem. 2018, 83, 6086
H. P. A. Khan, D. Das, T. K. Chakraborty
DOI: 10.1021/acs.joc.8b00752
CrossRef
chiral
racemic
Notes:
Terpenes

Sagittacin E

C14H18O4 = 250
Chem. Commun. 2018, 54, 6165
H. Abe, M. Fujimaki, E. Nakagawa, T. Kobayashi, H. Ito
DOI: 10.1039/C8CC03438A
CrossRef
chiral
racemic
Notes:
Terpenes

Sagittacin E, Acetyl-

C16H20O5 = 292
Chem. Commun. 2018, 54, 6165
H. Abe, M. Fujimaki, E. Nakagawa, T. Kobayashi, H. Ito
DOI: 10.1039/C8CC03438A
CrossRef
chiral
racemic
Notes:
Terpenes

Cardamom Peroxide

C20H28O5 = 348
Tetrahedron 2018, 74, 3358
X. Hu, P. Lim, R. M. Fairhurst, T. J. Maimone
DOI: 10.1016/j.tet.2018.03.045
CrossRef
chiral
racemic
Notes:
Terpenes

Higginsianin A

C27H38O4 = 426
J. Am. Chem. Soc. 2018, 140, 7462
R. R. Merchant, K. M. Oberg, Y. Lin, A. J. E. Novak, J. Felding, P. S. Baran
DOI: 10.1021/jacs.8b04891
CrossRef
chiral
racemic
Notes:
Terpenes

Subglutinol A

C27H38O4 = 426
J. Am. Chem. Soc. 2018, 140, 7462
R. R. Merchant, K. M. Oberg, Y. Lin, A. J. E. Novak, J. Felding, P. S. Baran
DOI: 10.1021/jacs.8b04891
CrossRef
chiral
racemic
Notes:
Terpenes

Subglutinol B

C27H38O4 = 426
J. Am. Chem. Soc. 2018, 140, 7462
R. R. Merchant, K. M. Oberg, Y. Lin, A. J. E. Novak, J. Felding, P. S. Baran
DOI: 10.1021/jacs.8b04891
CrossRef
chiral
racemic
Notes:
Terpenes

Salvinorin A

C23H28O8 = 432
Org. Lett. 2018, 20, 3418
Y. Wang, P. Metz
DOI: 10.1021/acs.orglett.8b01357
CrossRef
chiral
racemic
Notes:
79 data found. 1 - 30 listed Next Last