HeteroCycles

Search27,284 Compounds

Search by Journal: Journal Year

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

Natural Products with Heterocyclic Ring System

Synthesis

New Heterocyclic Natural Products

Updated: 20 December, 2019

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: All Polyketides Aromatics Terpenes Steroids Alkaloids Antibiotics Miscellaneous
Search by Journal: Angew. Chem. Int. Ed.Bull. Chem. Soc. Japan Chem. Commun.Chem. Eur. J.Chem. Pharm. Bull.Helv. Chim. Acta J. Am. Chem. Soc.J. Heterocycl. Chem.J. Org. Chem.Org. Biomol. Chem.Org. Lett.Synthesis Tetrahedron Tetrahedron Lett.
Year: 20192019201920192019201920192019201920192019201920192019
Vol: 58925525671021419256841721517560
No: 11-13322, 24143311, 12335, 6115, 661210, 12, 13

7 data found. 1 - 7 listed

Alkaloids

Leuvalin

C11H18N2O = 194

J. Org. Chem. 2019, 84, 3647

R. Ramesh, M. T. Bovino, Y. Zeng, J. Aubé

DOI: 10.1021/acs.joc.8b03206

CrossRef

chiral
racemic
Notes:

Alkaloids

Phevalin

C14H16N2O = 228

J. Org. Chem. 2019, 84, 3647

R. Ramesh, M. T. Bovino, Y. Zeng, J. Aubé

DOI: 10.1021/acs.joc.8b03206

CrossRef

chiral
racemic
Notes:

Alkaloids

Phileucin

C15H18N2O = 242

J. Org. Chem. 2019, 84, 3647

R. Ramesh, M. T. Bovino, Y. Zeng, J. Aubé

DOI: 10.1021/acs.joc.8b03206

CrossRef

chiral
racemic
Notes:

Alkaloids

Tyrvalin

C14H16N2O2 = 244

J. Org. Chem. 2019, 84, 3647

R. Ramesh, M. T. Bovino, Y. Zeng, J. Aubé

DOI: 10.1021/acs.joc.8b03206

CrossRef

chiral
racemic
Notes:

Alkaloids

Chilenamine

C20H21NO4 = 339

J. Org. Chem. 2019, 84, 2870

W. Zhu, S. Tong, J. Zhu, M.-X. Wang

DOI: 10.1002/ejoc.201900640

CrossRef

chiral
racemic
Notes:

Alkaloids

Palmanine

C21H21NO7 = 399

J. Org. Chem. 2019, 84, 2870

W. Zhu, S. Tong, J. Zhu, M.-X. Wang

DOI: 10.1002/ejoc.201900640

CrossRef

chiral
racemic
Notes:

Miscellaneous

Mozamide A

C45H64N8O8 = 844

J. Org. Chem. 2019, 84, 2489

L. Junk, U. Kazamaier

DOI: 10.1021/acs.joc.8b02836

CrossRef

chiral
racemic
Notes:

7 data found. 1 - 7 listed

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