Natural Products with Heterocyclic Ring System

Synthesis

New Heterocyclic Natural Products

Updated: 31 August, 2018

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

51 data found. 1 - 30 listed Next Last
Polyketides

Whisky Lactone, cis-

C9H16O2 = 156
Synlett 2017, 28, 2453
H. Xie, J. Lu, Y. Gui, L. Guo, Z. Song
DOI: 10.1055/s-0036-1588488
CrossRef
chiral
racemic
Notes:
Polyketides

Cognac Lactone, cis-

C10H18O2 = 170
Synlett 2017, 28, 2453
H. Xie, J. Lu, Y. Gui, L. Guo, Z. Song
DOI: 10.1055/s-0036-1588488
CrossRef
chiral
racemic
Notes:
Polyketides

Helicascolide C

C12H18O3 = 210
Tetrahedron Lett. 2017, 58, 4459
K. Zheng, C. Xie, R. Hong
DOI: 10.1016/j.tetlet.2017.10.021
CrossRef
chiral
racemic
Notes:
Polyketides

Felinone A

C11H16O4 = 212
Tetrahedron Lett. 2017, 58, 4296
H. Abe, H. Tango, T. Kobayashi, H. Ito
DOI: 10.1016/j.tetlet.2017.09.090
CrossRef
chiral
racemic
Notes: synthesis of enantiomer
Polyketides

Helicascolide A

C12H20O3 = 212
Tetrahedron Lett. 2017, 58, 4459
K. Zheng, C. Xie, R. Hong
DOI: 10.1016/j.tetlet.2017.10.021
CrossRef
chiral
racemic
Notes:
Polyketides

Helicascolide B

C12H20O3 = 212
Tetrahedron Lett. 2017, 58, 4459
K. Zheng, C. Xie, R. Hong
DOI: 10.1016/j.tetlet.2017.10.021
CrossRef
chiral
racemic
Notes:
Polyketides

Synargentolide B

C16H22O8 = 342
Tetrahedron 2017, 73, 6443
J. Liu, Y. Gao, L. Wang, Y. Du
DOI: 10.1016/j.tet.2017.09.041
CrossRef
chiral
racemic
Notes:
Aromatics

Heliannuol G

C15H20O3 = 248
Tetrahedron Lett. 2017, 58, 4336
D. Sarkar, M. K. Ghosh
DOI: 10.1016/j.tetlet.2017.09.081
CrossRef
chiral
racemic
Notes:
Aromatics

Monocillin II

C18H20O5 = 316
Org. Lett. 2017, 19, 6004
H. Choe, H. Cho, H.-J. Ko, J. Lee
DOI: 10.1021/acs.orglett.7b03054
CrossRef
chiral
racemic
Notes:
Aromatics

Pochonin D

C18H19O5Cl = 350.5
Org. Lett. 2017, 19, 6004
H. Choe, H. Cho, H.-J. Ko, J. Lee
DOI: 10.1021/acs.orglett.7b03054
CrossRef
chiral
racemic
Notes:
Aromatics

Dendrochrysanene

C30H20O8 = 508
J. Org. Chem. 2017, 82, 11573
N. Katsuki, S. Isshiki, D. Fukatsu, J. Okamura, K. Kuramochi, T. Kawabata, K. Tsubaki
DOI: 10.1021/acs.joc.7b02223
CrossRef
chiral
racemic
Notes:
Aromatics

Theaflavin

C29H24O12 = 564
Synlett 2017, 28, 2505
Y. Matsuo, R. Oowatashi, Y. Saito, T. Tanaka
DOI: 10.1055/s-0036-1588529
CrossRef
chiral
racemic
Notes:
Aromatics

Theaflavin, Neo-

C29H24O12 = 564
Synlett 2017, 28, 2505
Y. Matsuo, R. Oowatashi, Y. Saito, T. Tanaka
DOI: 10.1055/s-0036-1588529
CrossRef
chiral
racemic
Notes:
Aromatics

Perviridisin B

C36H42N2O9 = 646
Angew. Chem. Int. Ed. 2017, 56, 14479
W. W. A. Clay, R. Krishnan, N. J. Lajkiewicz, L. E. Brown, J. Sivaguru, J. A. Porco, Jr.
DOI: 10.1002/anie.201707539
CrossRef
chiral
racemic
Notes:
Aromatics

Lagerstannin C

C27H21O19 = 650
Synthesis 2017, 49, 5003
Y. Kaneko, S. Wakamori, K. Ikeuchi, K. Ohara, T. Tanaka, H. Yamada
DOI: 10.1055/s-0036-1588477
CrossRef
chiral
racemic
Notes:
Aromatics

Foveoglin A

C38H40N2O8 = 652
Angew. Chem. Int. Ed. 2017, 56, 14479
W. W. A. Clay, R. Krishnan, N. J. Lajkiewicz, L. E. Brown, J. Sivaguru, J. A. Porco, Jr.
DOI: 10.1002/anie.201707539
CrossRef
chiral
racemic
Notes: formal synthesis and synthesis of enantionmer
Aromatics

Theaflavin-3-O-gallate

C36H28O16 = 716
Synlett 2017, 28, 2505
Y. Matsuo, R. Oowatashi, Y. Saito, T. Tanaka
DOI: 10.1055/s-0036-1588529
CrossRef
chiral
racemic
Notes:
Terpenes

Asteriscunolide C

C15H18O3 = 246
Synth. Commun. 2017, 47, 2103
R. A. Fernandes, V. P. Chavan, A. Panja
DOI: 10.1080/00397911.2017.1365907
CrossRef
chiral
racemic
Notes:
Terpenes

Paralemnolide A

C15H22O5 = 282
Org. Lett. 2017, 19, 5996
H. Abe, Y. Ogura, T. Kobayashi, H. Ito
DOI: 10.1021/acs.orglett.7b03038
CrossRef
chiral
racemic
Notes:
Terpenes

Resinferatoxin

C37H40O9 = 628
J. Am. Chem. Soc. 2017, 139, 16420
S. Hashimoto, S. Katoh, T. Kato, D. Urabe, M. Inoue
DOI: 10.1021/jacs.7b10177
CrossRef
chiral
racemic
Notes:
Alkaloids

LAB-1

C5H11NO3 = 133
Synthesis 2017, 49, 4869
E. C. de Silva, N. C. G, Yamakawa, A. A. Dos Santos, F. Coelho
DOI: 10.1055/s-0036-1590799
CrossRef
chiral
racemic
Notes:
Alkaloids

Monomorine I

C13H25N = 195
Tetrahedron Asymmetry 2017, 28, 1582
M. Asai, Y. Takemoto, A. Deguchi, Y. Hattori, H. Makabe
DOI: 10.1016/j.tetasy.2017.09.008
CrossRef
chiral
racemic
Notes:
Alkaloids

Eustifoline D

C15H11NO = 221
Tetrahedron Lett. 2017, 58, 4328
R. A. Aitken, L. Murray
DOI: 10.1016/j.tetlet.2017.09.073
CrossRef
chiral
racemic
Notes:
Alkaloids

Aspidospermidine

C19H26N2 = 282
Org. Lett. 2017, 19, 6168
J.-Y. Kim, C.-H. Suhl, J.-H. Lee, C.-G. Cho
DOI: 10.1021/acs.orglett.7b03078
CrossRef
chiral
racemic
Notes: formal synthesis
Alkaloids

Rosettacin

C19H12N2O = 284
Chem. Commun. 2017, 53, 12394
L. Song, G. Tian, Y. He, E. V. Van der Eycken
DOI: 10.1039/C7CC06860C
CrossRef
chiral
racemic
Notes:
Alkaloids

Lycoricidine

C14H13NO6 = 291
Tetrahedron 2017, 73, 6773
P. Saidhareddy, A. K. Shaw
DOI: 10.1016/j.tet.2017.10.033
CrossRef
chiral
racemic
Notes:
Alkaloids

Lycoricidine

C14H13NO6 = 291
Angew. Chem. Int. Ed. 2017, 56, 15049
E. H. Southgate, D. R. Holycross, D. Sarlah
DOI: 10.1002/anie.201709712
CrossRef
chiral
racemic
Notes:
Alkaloids

Narciclasine

C14H13NO7 = 307
Angew. Chem. Int. Ed. 2017, 56, 15049
E. H. Southgate, D. R. Holycross, D. Sarlah
DOI: 10.1002/anie.201709712
CrossRef
chiral
racemic
Notes:
Alkaloids

Pancratistatin, 7-Deoxy-

C14H11NO7 = 309
J. Am. Chem. Soc. 2017, 139, 15656
L. W. Hernandez, J. Pospech, U. Klöckner, T. W. Bingham, D. Sarlah
DOI: 10.1021/jacs.7b10351
CrossRef
chiral
racemic
Notes:
Alkaloids

Akuammicine

C20H22N2O2 = 322
Chem. Eur. J. 2017, 23, 16189
G. S. Lee, G. Namkoong, J. Park, D. Y.‐K. Chen
DOI: 10.1002/chem.201704455
CrossRef
chiral
racemic
Notes:
51 data found. 1 - 30 listed Next Last