HETEROCYCLES

An International Journal for Reviews and Communications in Heterocyclic Chemistry
Web Edition ISSN: 1881-0942
Published online by The Japan Institute of Heterocyclic Chemistry

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Search27,284 Compounds

Nomenclature:

The natural products are listed under the name used in the original literature.

The abbreviations:

The following abbreviations have been used:

• act:
• biological activity

• cd:
• circular dichroism

• Cnmr:
• 13C-nuclear magnetic resonance spectrum

• Hnmr:
• 1H-nuclear magnetic resonance spectrum

• ir:
• infrared spectrum

• mass:
• mass spectrum

• syn:
• total synthesis

• uv:
• ultraviolet spectrum

Journal:

This database lists the natural products with heterocyclic ring system whose synthesis has been determined since 1975. The journals which have been covered are as follows:

Angew. Chem. Int. Ed. Engl.
Angew. Chem. Int. Ed.
Bull. Chem. Soc. Japan
Chem. and Ind.
Chem. Ber.
J. Chem. Soc., Chem. Commun.
Chem. Commun.
Chem. Eur. J.
Chemistry Lett.
Chem. Pharm. Bull.
Coll. Czech. Chem. Commun.
Eur. J. Inorg. Chem.
Eur. J. Org. Chem.
Experientia
Helv. Chim. Acta
Heterocycles
J. Am. Chem. Soc.
J. Antibiot.
J. Chem. Soc., Perkin Trans. 1
J. Heterocycl. Chem.
J. Med. Chem.
J. Nat. Prod.
J. Org. Chem.
J. Pharm. Sci.
Liebigs Ann. Chem.
Monatsh. Chem.
Org. Lett.
Phytochemistry
Planta medica
Synlett
Synth. Commun.
Synthesis
Tetrahedron
Tetrahedron Asymmetry
Tetrahedron Lett.
Yakugaku Zasshi

Editor:

Editor:
Kunio Ogasawara

Associate Editors:
Toshio Honda

Editorial Assistants:
Sayaka Kametani
Seiya Kametani
Saki Kida
Kaori Tsuji

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

• Search by Group: AllPolyketidesAromaticsTerpenesSteroidsAlkaloidsAntibioticsMiscellaneous
• Search by Journal: Angew. Chem. Int. Ed.Bull. Chem. Soc. JapanChem. Commun.Chem. Eur. J.Chem. Pharm. Bull.Helv. Chim. ActaJ. Am. Chem. Soc.J. Heterocycl. Chem.J. Org. Chem.Org. Biomol. Chem.Org. Lett.SynthesisTetrahedronTetrahedron Lett.
• Year: 20192019201920192019201920192019201920192019201920192019
• Vol: 58925525671021419256841721517560
• No: 11-13322, 24143311, 12335, 6115, 661210, 12, 13

Terpenes

Rhodomyrtusial A

C30H44O4 = 468

Angew. Chem. Int. Ed. 2019, 58, 4291

X.-J. Qin, T. J. Rauwolf, P.-P. Li, H. Liu, J. McNeely, Y. Hua, H.-Y. Liu, J. A. Porco, Jr.

DOI: 10.1002/anie.201981713

CrossRef

chiral
racemic
Notes:

Terpenes

Rhodomyrtusial C

C30H44O4 = 468

Angew. Chem. Int. Ed. 2019, 58, 4291

X.-J. Qin, T. J. Rauwolf, P.-P. Li, H. Liu, J. McNeely, Y. Hua, H.-Y. Liu, J. A. Porco, Jr.

DOI: 10.1002/anie.201814421

CrossRef

chiral
racemic
Notes:

Terpenes

Rhotomentodione A

C30H44O4 = 468

Angew. Chem. Int. Ed. 2019, 58, 4291

X.-J. Qin, T. J. Rauwolf, P.-P. Li, H. Liu, J. McNeely, Y. Hua, H.-Y. Liu, J. A. Porco, Jr.

DOI: 10.1002/anie.201814421

CrossRef

chiral
racemic
Notes:

Terpenes

Rhotomentodione B

C30H44O4 = 468

Angew. Chem. Int. Ed. 2019, 58, 4291

X.-J. Qin, T. J. Rauwolf, P.-P. Li, H. Liu, J. McNeely, Y. Hua, H.-Y. Liu, J. A. Porco, Jr.

DOI: 10.1002/anie.201981713

CrossRef

chiral
racemic
Notes:

Terpenes

Tomentodione Q

C30H44O4 = 468

Angew. Chem. Int. Ed. 2019, 58, 4291

X.-J. Qin, T. J. Rauwolf, P.-P. Li, H. Liu, J. McNeely, Y. Hua, H.-Y. Liu, J. A. Porco, Jr.

DOI: 10.1002/anie.201981713

CrossRef

chiral
racemic
Notes:

Terpenes

Tomentodione R

C30H44O4 = 468

Angew. Chem. Int. Ed. 2019, 58, 4291

X.-J. Qin, T. J. Rauwolf, P.-P. Li, H. Liu, J. McNeely, Y. Hua, H.-Y. Liu, J. A. Porco, Jr.

DOI: 10.1002/anie.201981713

CrossRef

chiral
racemic
Notes:

Alkaloids

Chimonamidine

C12H16N2O2 = 220

Angew. Chem. Int. Ed. 2019, 58, 3402

M. Moskowitz, C. Wolf

DOI: 10.1002/anie.201981713

CrossRef

chiral
racemic
Notes:

Alkaloids

Gephyrotoxin

C19H29NO = 287

Angew. Chem. Int. Ed. 2019, 58, 3809

Y. Chen, Y.-M. He, S. Zhang, T. Miao, Q.-H. Fan

DOI: 10.1002/anie.201981713

CrossRef

chiral
racemic
Notes:	formal synthesis

Alkaloids

Cylindricine C

C19H33NO2 = 307

Angew. Chem. Int. Ed. 2019, 58, 4381

S. Hiraoka, T. Matsumoto, K. Matsuzaka, T. Sato, N. Chida

DOI: 10.1002/anie.201981713

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:

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