Natural Products with Heterocyclic Ring System

Synthesis

New Heterocyclic Natural Products

Updated: 4 April, 2018

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

90 data found. 1 - 30 listed Next Last
Polyketides

Dendrodolide L

C12H20O4 = 228
Tetrahedron Lett. 2017, 58, 2344
V. R. Regalla, R. R. Addada, V. S. Puli, A. S. Saxena, A. Chatterjee
DOI: 10.1016/j.tetlet.2017.04.097
CrossRef
chiral
racemic
Notes:
Polyketides

Methynolide

C17H28O5 = 312
Tetrahedron 2017, 73, 3652
T. Suzuki, M. Fujimura, K. Fujita, S. Kobayashi
DOI: 10.1016/j.tet.2017.03.093
CrossRef
chiral
racemic
Notes:
Polyketides

Glabramycin B

C22H26O6 = 386
Tetrahedron 2017, 73, 3271
M. Yamamoto, K. Ishigami, H. Watanabe
DOI: 10.1016/j.tet.2017.04.061
CrossRef
chiral
racemic
Notes:
Aromatics

Equol

C15H14O3 = 242
Org. Lett. 2017, 19, 2981
T. Qin, P. Metz
DOI: 10.1021/acs.orglett.7b01218
CrossRef
chiral
racemic
Notes: formal synthesis synthesis of enantiomer
Aromatics

Daidzein, Dihydro-

C15H12O4 = 256
Org. Lett. 2017, 19, 2981
T. Qin, P. Metz
DOI: 10.1021/acs.orglett.7b01218
CrossRef
chiral
racemic
Notes:
Aromatics

No Name

C18H30O3 = 294
Adv. Synth. Catal. 2017, 359, 1811
W. Huang, C. Liu, Y. Gu
DOI: 10.1002/adsc.201700074
CrossRef
chiral
racemic
Notes:
Aromatics

Morin

C15H10O7 = 302
Tetrahedron 2017, 73, 3485
X. Sheng, X.-Y. Jia, F. Tang, Y. Wang, A.-J. Hou
DOI: 10.1016/j.tet.2017.05.022
CrossRef
chiral
racemic
Notes:
Aromatics

Thymarnicol

C20H20O4 = 324
Angew. Chem. Int. Ed. 2017, 56, 6813
I. De Silvestro, S. L. Drew, G. S. Nichol, F. Duarte, A. L. Lawrence
DOI: 10.1002/anie.201701481
CrossRef
chiral
racemic
Notes:
Aromatics

Kidamycinone

C22H16O5 = 360
J. Org. Chem. 2017, 82, 5710
T. Mabit, A. Siard, M. Pantin, D. Zon, L. Foulgoc, D. Sissouma, A. Guingant, M. Mathé-Allainmat, J. Lebreton, F. Carreaux, G. Dujardin, S. Collet
DOI: 10.1021/acs.joc.7b00544
CrossRef
chiral
racemic
Notes:
Aromatics

γ-Indomycinone

C22H18O6 = 378
J. Org. Chem. 2017, 82, 5710
T. Mabit, A. Siard, M. Pantin, D. Zon, L. Foulgoc, D. Sissouma, A. Guingant, M. Mathé-Allainmat, J. Lebreton, F. Carreaux, G. Dujardin, S. Collet
DOI: 10.1021/acs.joc.7b00544
CrossRef
chiral
racemic
Notes:
Aromatics

Neomarchantin A

C28H24O4 = 424
Org. Lett. 2017, 19, 2889
É. Morin, M. Raymond, A. Dubart, S. K. Collins
DOI: 10.1021/acs.orglett.7b01127
CrossRef
chiral
racemic
Notes:
Aromatics

Sanggenol F

C26H28O6 = 436
Tetrahedron 2017, 73, 3485
X. Sheng, X.-Y. Jia, F. Tang, Y. Wang, A.-J. Hou
DOI: 10.1016/j.tet.2017.05.022
CrossRef
chiral
racemic
Notes:
Terpenes

Perforanoid A

C25H28O6 = 424
Tetrahedron 2017, 73, 3612
C. Lv, Q. Tu, J. Gong, X. Hao, Z. Yang
DOI: 10.1016/j.tet.2017.03.072
CrossRef
chiral
racemic
Notes:
Terpenes

Myrtucommulone K

C29H44O3 = 440
Tetrahedron 2017, 73, 3691
L. Lv, Y. Li, Y. Zhang, Z. Xie
DOI: 10.1016/j.tet.2017.05.007
CrossRef
chiral
racemic
Notes:
Terpenes

Myrtucommulone N

C29H44O3 = 440
Tetrahedron 2017, 73, 3691
L. Lv, Y. Li, Y. Zhang, Z. Xie
DOI: 10.1016/j.tet.2017.05.007
CrossRef
chiral
racemic
Notes:
Terpenes

Myrtucommulone O

C29H44O3 = 440
Tetrahedron 2017, 73, 3691
L. Lv, Y. Li, Y. Zhang, Z. Xie
DOI: 10.1016/j.tet.2017.05.007
CrossRef
chiral
racemic
Notes:
Terpenes

Echinoside B

C41H65O16NaS = 868
Angew. Chem. Int. Ed. 2017, 56, 7648
X. Chen, X. Shao, W. Li, X. Zhang, B. Yu
DOI: 10.1002/anie.201703610
CrossRef
chiral
racemic
Notes: Na salt
Terpenes

Echinoside A, Ds-

C54H88O23 = 1104
Angew. Chem. Int. Ed. 2017, 56, 7648
X. Chen, X. Shao, W. Li, X. Zhang, B. Yu
DOI: 10.1002/anie.201703610
CrossRef
chiral
racemic
Notes:
Terpenes

Echinoside A

C54H87O26NaS = 1206
Angew. Chem. Int. Ed. 2017, 56, 7648
X. Chen, X. Shao, W. Li, X. Zhang, B. Yu
DOI: 10.1002/anie.201703610
CrossRef
chiral
racemic
Notes: Na salt
Alkaloids

Hyacinthacine B4

C9H17NO4 = 203
J. Org. Chem. 2017, 82, 5835
T. Pecchioli, F. Cardona, H.-U. Reissig, R. Zimmer
DOI: 10.1021/acs.joc.7b00667
CrossRef
chiral
racemic
Notes:
Alkaloids

Sorazolon E

C14H13NO = 211
Chem. Asian J. 2017, 12, 1305
M. Sato, K. Ichinose, S. Takizawa, H. Sasai
DOI: 10.1002/asia.201700471
CrossRef
chiral
racemic
Notes:
Alkaloids

Hyacinthacine C5

C9H17NO5 = 219
J. Org. Chem. 2017, 82, 5835
T. Pecchioli, F. Cardona, H.-U. Reissig, R. Zimmer
DOI: 10.1021/acs.joc.7b00667
CrossRef
chiral
racemic
Notes:
Alkaloids

Carbazomycin B, 4-Deoxy-

C15H15NO = 225
Chem. Asian J. 2017, 12, 1305
M. Sato, K. Ichinose, S. Takizawa, H. Sasai
DOI: 10.1002/asia.201700471
CrossRef
chiral
racemic
Notes:
Alkaloids

Peramine

C11H15N5O = 233
Tetrahedron 2017, 73, 3443
Y. Yamamoto, A. Nakazaki, T. Nishikawa
DOI: 10.1016/j.tet.2017.05.004
CrossRef
chiral
racemic
Notes: TFA salt
Alkaloids

Costaclavine

C16H20N2 = 240
Org. Lett. 2017, 19, 3323
H. Liu, X. Zhang, D. Shan, M. Pitchakuntla, Y. Ma, Y. Jia
DOI: 10.1021/acs.orglett.7b01504
CrossRef
chiral
racemic
Notes:
Alkaloids

Costaclavine, epi-

C16H20N2 = 240
Org. Lett. 2017, 19, 3323
H. Liu, X. Zhang, D. Shan, M. Pitchakuntla, Y. Ma, Y. Jia
DOI: 10.1021/acs.orglett.7b01504
CrossRef
chiral
racemic
Notes:
Alkaloids

Festuclavine

C16H20N2 = 240
Org. Lett. 2017, 19, 3323
H. Liu, X. Zhang, D. Shan, M. Pitchakuntla, Y. Ma, Y. Jia
DOI: 10.1021/acs.orglett.7b01504
CrossRef
chiral
racemic
Notes:
Alkaloids

Pyrocalvine

C16H20N2 = 240
Org. Lett. 2017, 19, 3323
H. Liu, X. Zhang, D. Shan, M. Pitchakuntla, Y. Ma, Y. Jia
DOI: 10.1021/acs.orglett.7b01504
CrossRef
chiral
racemic
Notes:
Alkaloids

Carbazomycin B

C15H15NO2 = 241
Adv. Synth. Catal. 2017, 359, 1860
A. Banerjee, S. Sahu, M. S. Maji
DOI: 10.1002/adsc.201700092
CrossRef
chiral
racemic
Notes: formal synthesis
Alkaloids

Usabamycin C

C15H18N2O = 242
Tetrahedron Lett. 2017, 58, 2426
G. Sakaine, R. Zemribo, G. Smits
DOI: 10.1016/j.tetlet.2017.05.020
CrossRef
chiral
racemic
Notes:
90 data found. 1 - 30 listed Next Last