Natural Products with Heterocyclic Ring System

Synthesis

New Heterocyclic Natural Products

Updated: 26 December, 2017

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

61 data found. 1 - 30 listed Next Last
Polyketides

No. 2106 A

C8H10O4 = 170
Eur. J. Org. Chem. 2017, , 1323
S. Grélaud, J. Lusseau, Y. Landais
DOI: 10.1002/ejoc.201601624
CrossRef
chiral
racemic
Notes:
Polyketides

Decarestrictine H

C10H14O4 = 198
Tetrahedron 2017, 73, 1733
R. Katsuta, N. Masada, Y. Shimodaira, S. Ueda, A. Yajima, T. Nukada
DOI: 10.1016/j.tet.2017.02.023
CrossRef
chiral
racemic
Notes:
Polyketides

Decarestrictine J

C10H16O4 = 200
Tetrahedron 2017, 73, 1733
R. Katsuta, N. Masada, Y. Shimodaira, S. Ueda, A. Yajima, T. Nukada
DOI: 10.1016/j.tet.2017.02.023
CrossRef
chiral
racemic
Notes:
Polyketides

Pestalotioprolide C

C14H24O4 = 256
Tetrahedron Lett. 2017, 58, 1198
K. S. N. Reddy, G. Sabitha
DOI: 10.1016/j.tetlet.2017.02.019
CrossRef
chiral
racemic
Notes:
Polyketides

Goniothalesdiol A

C14H18O5 = 266
Tetrahedron Lett. 2017, 58, 1037
P. Ramesh, Y. N. Reddy
DOI: 10.1016/j.tetlet.2017.01.100
CrossRef
chiral
racemic
Notes:
Polyketides

Ramariolide C

C16H26O3 = 266
Org. Lett. 2017, 19, 1164
P. Pal, S. Nanda
DOI: 10.1021/acs.orglett.7b00202
CrossRef
chiral
racemic
Notes:
Polyketides

Ramariolide A

C16H26O4 = 282
Org. Lett. 2017, 19, 1164
P. Pal, S. Nanda
DOI: 10.1021/acs.orglett.7b00202
CrossRef
chiral
racemic
Notes:
Polyketides

Clavilactone D

C16H15NO5 = 301
Chem. Eur. J. 2017, 23, 3828
K. Takao, R. Nemoto, K. Mori, A. Namba, K. Yoshida, A. Ogura
DOI: 10.1002/chem.201700483
CrossRef
chiral
racemic
Notes:
Polyketides

Pipoxide

C21H18O6 = 366
Tetrahedron Lett. 2017, 58, 1075
A. Vinaykumar, C. Muniraju, B. V. Rao
DOI: 10.1016/j.tetlet.2017.02.003
CrossRef
chiral
racemic
Notes: formal synthesis
Polyketides

Thyrsiferol, Isodehydro-

C30H51O6Br = 587
Angew. Chem. Int. Ed. 2017, 56, 3064
A. Hoshino, H. Nakai, M. Morino, K. Nishikawa, T. Kodama, K. Nishikibe, Y. Morimoto
DOI: 10.1002/anie.201611829
CrossRef
chiral
racemic
Notes: synthesis of both enantiomers
Polyketides

Marinisporolide C

C38H58O10 = 674
J. Org. Chem. 2017, 82, 3019
L. C. Dias, E. C. de Lucca, Jr.
DOI: 10.1021/acs.joc.7b00023
CrossRef
chiral
racemic
Notes:
Aromatics

Avicequinone C

C15H12O4 = 256
Chem. Pharm. Bull. 2017, 65, 253
W. Karnsomwan, P. Netcharoensirisuk, T. Rungrotmongkol, W. De-Eknamkul, S. Chamni
DOI: 10.1248/cpb.c16-00727
CrossRef
chiral
racemic
Notes:
Aromatics

Kehokorin D

C19H14O4 = 306
J. Org. Chem. 2017, 82, 3159
S. Takahashi, Y. Suda, T. Nakamura, K. Matsuoka, H. Koshino
DOI: 10.1021/acs.joc.7b00147
CrossRef
chiral
racemic
Notes:
Aromatics

Kehokorin E

C20H16O4 = 320
J. Org. Chem. 2017, 82, 3159
S. Takahashi, Y. Suda, T. Nakamura, K. Matsuoka, H. Koshino
DOI: 10.1021/acs.joc.7b00147
CrossRef
chiral
racemic
Notes:
Aromatics

Kehokorin C

C21H18O5 = 336
J. Org. Chem. 2017, 82, 3159
S. Takahashi, Y. Suda, T. Nakamura, K. Matsuoka, H. Koshino
DOI: 10.1021/acs.joc.7b00147
CrossRef
chiral
racemic
Notes:
Aromatics

Kehokorin B

C21H18O6 = 366
J. Org. Chem. 2017, 82, 3159
S. Takahashi, Y. Suda, T. Nakamura, K. Matsuoka, H. Koshino
DOI: 10.1021/acs.joc.7b00147
CrossRef
chiral
racemic
Notes:
Aromatics

Catechin, 6-(2”-Pyrolidinone-5”-yl)-epi-

C19H19NO7 = 373
Tetrahedron 2017, 73, 1503
V. Ilkei, A. Spaits, A. Prechl, J. Müller, Á. Könczöl, S. Lévai, E. Riethmüller, Á. Szigetvári, Z. Béni, M. Dékány, A. Martins, A. Hunyadi, S. Antus, C. Szántay Jr., G. T. Balogh, G. Kalaus, H. Bölcskei, L. Hazai
DOI: 10.1016/j.tet.2017.01.068
CrossRef
chiral
racemic
Notes:
Aromatics

Catechin, 8-(2”-Pyrolidinone-5”-yl)-epi-

C19H19NO7 = 373
Tetrahedron 2017, 73, 1503
V. Ilkei, A. Spaits, A. Prechl, J. Müller, Á. Könczöl, S. Lévai, E. Riethmüller, Á. Szigetvári, Z. Béni, M. Dékány, A. Martins, A. Hunyadi, S. Antus, C. Szántay Jr., G. T. Balogh, G. Kalaus, H. Bölcskei, L. Hazai
DOI: 10.1016/j.tet.2017.01.068
CrossRef
chiral
racemic
Notes:
Aromatics

Quercetin, 8-(2”-Pyrolidinone-5”-yl)-

C19H15NO8 = 385
Tetrahedron 2017, 73, 1503
V. Ilkei, A. Spaits, A. Prechl, J. Müller, Á. Könczöl, S. Lévai, E. Riethmüller, Á. Szigetvári, Z. Béni, M. Dékány, A. Martins, A. Hunyadi, S. Antus, C. Szántay Jr., G. T. Balogh, G. Kalaus, H. Bölcskei, L. Hazai
DOI: 10.1016/j.tet.2017.01.068
CrossRef
chiral
racemic
Notes:
Aromatics

Kehokorin A

C27H28O10 = 512
J. Org. Chem. 2017, 82, 3159
S. Takahashi, Y. Suda, T. Nakamura, K. Matsuoka, H. Koshino
DOI: 10.1021/acs.joc.7b00147
CrossRef
chiral
racemic
Notes:
Aromatics

Actinorhodin, γ-

C32H22O14 = 630
Angew. Chem. Int. Ed. 2017, 56, 3383
M. Neumeyer, R. Brückner
DOI: 10.1002/anie.201611183
CrossRef
chiral
racemic
Notes:
Terpenes

Amphilectolide

C17H24O2 = 260
J. Am. Chem. Soc. 2017, 139, 4117
H.-D. Hao, D. Trauner
DOI: 10.1021/jacs.7b00234
CrossRef
chiral
racemic
Notes:
Terpenes

Caribenol A

C19H26O3 = 302
J. Am. Chem. Soc. 2017, 139, 4117
H.-D. Hao, D. Trauner
DOI: 10.1021/jacs.7b00234
CrossRef
chiral
racemic
Notes: formal synthesis
Terpenes

Aplykurodinone-1

C20H30O3 = 318
Org. Lett. 2017, 19, 1056
C. Tao, J. Zhang, X. Chen, H. Wang, Y. Li, B. Cheng, H. Zhai
DOI: 10.1021/acs.orglett.7b00068
CrossRef
chiral
racemic
Notes: formal synthesis
Terpenes

Kalihinol C

C22H32N2O2 = 356
J. Am. Chem. Soc. 2017, 139, 3647
C. A. Reiher, R. A. Shenvi
DOI: 10.1021/jacs.7b00854
CrossRef
chiral
racemic
Notes:
Terpenes

Lungshengenin D

C22H32O5 = 376
J. Am. Chem. Soc. 2017, 139, 2932
X. Zhao, W. Li, J. Wang, D. Ma
DOI: 10.1021/jacs.7b00140
CrossRef
chiral
racemic
Notes:
Steroids

Cardenolide N-1

C30H46O7 = 518
J. Org. Chem. 2017, 82, 3327
J. Mestre, M. I. Matheu, Y. Díaz, S. Castillón, O. Boutureira
DOI: 10.1021/acs.joc.7b00210
CrossRef
chiral
racemic
Notes:
Alkaloids

Trisphaeridine

C14H9NO2 = 223
J. Heterocycl. Chem. 2017, 54, 1645
Y. Kuwata, M. Sonoda, S. Tanimori
DOI: 10.1002/jhet.2725
CrossRef
chiral
racemic
Notes:
Alkaloids

Cytoxazole

C12H15NO4 = 237
Tetrahedron 2017, 73, 1473
M. Lingamurthy, G. R. Nalliboina, M. V. Rao, B. S. Reddy, H. M. S. Kumar
DOI: 10.1016/j.tet.2017.01.059
CrossRef
chiral
racemic
Notes:
Alkaloids

Bicolorine

C15H12NO2 = 238
J. Heterocycl. Chem. 2017, 54, 1645
Y. Kuwata, M. Sonoda, S. Tanimori
DOI: 10.1002/jhet.2725
CrossRef
chiral
racemic
Notes: I salt
61 data found. 1 - 30 listed Next Last