Heterocycles Database
Total Synthesis of
Heterocyclic
Natural Products
 
 1975-2014
 19,943 Compounds
 27 April, 2012
 
Search by:
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Carbon
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Group

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Molecular Weight:

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Journal
Year
 
 Nomenclature :
 
The natural products are listed under the name used in the original literature.
 
 Journals :
 
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
Keiichiro Fukumoto

Associate Editor
Kunio Ogasawara
Yoshiharu Iwabuchi

Assistant Editors
Naoki Kanoh
Muneo Kawasumi
Takashi Moriya
Keiichi Murakami
Kohei Sakanishi
Yusuke Sasano
Takuro Shibuta
Masatoshi Shibuya

Editorial Assistants
Sayaka Kametani
Kishiko Nakano
Yuki Shima
Kazuko Todoroki
Michi Yamamoto
 New Total Synthesis of Heterocyclic Natural Products
This journal will list natural products with heterocyclic ring system whose total synthesis has been reported.
 
27 April, 2012
Search by Group:
Polyketides
Aromatics
Terpenes
Steroids
Alkaloids
Antibiotics
Miscellaneous
 
All
 
Search by Journal :
Vol.
No.
Angew. Chem. Int. Ed.
50
37-40
Chem. Commun.
47
35, 36
Eur. J. Org. Chem.
2011
25, 26
J. Nat. Prod.
74
9
J. Org. Chem.
76
17
Org. Bio. Chem.
9
18
Org. Lett.
13
17, 18
Synlett
2011
14, 15
Synthesis
2011
17, 18
Tetrahedron
67
35, 36, 38, 39
Tetrahedron Lett.
52
36-38
  63 data found. 1 - 30 listed Next Last   

Polyketides
Ophiocerin C
C6H12O3 = 132
Helv. Chim. Acta    2014, 97 , 491
J. S. Yadav, N. M. Reddy, M. A. Rahman, A. M. Reddy, A. R. Prasad
DOI: 10.1002/hlca.201300203
CrossRef
 
chiral
racemic
Notes:


Polyketides
Botryolide E
C10H14O5 = 214
Helv. Chim. Acta    2014, 97 , 491
J. S. Yadav, N. M. Reddy, M. A. Rahman, A. M. Reddy, A. R. Prasad
DOI: 10.1002/hlca.201300203
CrossRef
 
chiral
racemic
Notes:


Polyketides
Decytospolide A
C14H26O3 = 242
Tetrahedron Lett.    2014, 55 , 2221
D. Clarisse, F. Fache
DOI: 10.1016/j.tetlet.2014.02.060
CrossRef
 
chiral
racemic
Notes:


Polyketides
Boronolide, Deacetyl-
C12H20O5 = 244
Tetrahedron Lett.    2014, 55 , 2822
Y. Kurogome, Y. Hattori, H. Makabe
DOI: 10.1016/j.tetlet.2014.03.070
CrossRef
 
chiral
racemic
Notes:


Polyketides
Decytospolide B
C16H28O4 = 284
Tetrahedron Lett.    2014, 55 , 2221
D. Clarisse, F. Fache
DOI: 10.1016/j.tetlet.2014.02.060
CrossRef
 
chiral
racemic
Notes:


Polyketides
PsiAβ
C18H32O3 = 296
Synlett    2014, 25 , 975
P. R. Reddy, M. Lingaiah, B. Das
DOI: 10.1055/s-0033-1340834
CrossRef
 
chiral
racemic
Notes:


Polyketides
Zooxanthellactone
C22H30O2 = 326
Tetrahedron Lett.    2014, 55 , 2842
M. G. Jakobsen, A. Vik, T. V. Hansen
DOI: 10.1016/j.tetlet.2014.03.085
CrossRef
 
chiral
racemic
Notes:


Polyketides
Laurepinnacin, Iso-
C15H20OClBr = 331.5
Chem. Commun.    2014, 50 , 3685
J. Rodríguez-López, N. Ortega, V. S. Martín, T. Martín
DOI: 10.1039/c4cc00389f
CrossRef
 
chiral
racemic
Notes: formal synthesis, (+)-enantiomer


Polyketides
Rogioloxepane A
C15H20OClBr = 331.5
Chem. Commun.    2014, 50 , 3685
J. Rodríguez-López, N. Ortega, V. S. Martín, T. Martín
DOI: 10.1039/c4cc00389f
CrossRef
 
chiral
racemic
Notes: formal synthesis, (+)-enantiomer


Polyketides
Boronolide
C18H26O8 = 370
Tetrahedron Lett.    2014, 55 , 2822
Y. Kurogome, Y. Hattori, H. Makabe
DOI: 10.1016/j.tetlet.2014.03.070
CrossRef
 
chiral
racemic
Notes:


Polyketides
Xyolide
C20H32O8 = 400
Tetrahedron    2014, 70 , 2634
R. K. Rej, A. Jana, S. Nanda
DOI: 10.1016/j.tet.2014.02.072
CrossRef
 
chiral
racemic
Notes:


Polyketides
Kendomycin
C29H42O6 = 486
Angew. Chem. Int. Ed.    2014, 53 , 4213
T. Sengoku, S. Xu, K. Ogura, Y. Emori, K. Kitada, D. Uemura, H. Arimoto
DOI: 10.1002/anie.201400305
CrossRef
 
chiral
racemic
Notes:


Polyketides
Kendomycin
C29H42O6 = 486
Chem. Eur. J.    2014, 20 , 4396
L. Hoffmeister, P. Persich, A. Früstner
DOI: 10.1002/chem.201304580
CrossRef
 
chiral
racemic
Notes: formal synthesis


Polyketides
Mandelalide A
C33H52O11 = 624
Angew. Chem. Int. Ed.    2014, 53 , 4217
J. Willwacher, A. Fürstner
DOI: 10.1002/anie.201400605
CrossRef
 
chiral
racemic
Notes: proposed structure


Aromatics
Aspergillumarin A
C14H16O4 = 248
Tetrahedron Lett.    2014, 55 , 2921
J. S. Yadav, A. K. Mishra, S. S. Dachavaram, S. G. Kumar, S. Das
DOI: 10.1016/j.tetlet.2014.03.067
CrossRef
 
chiral
racemic
Notes:


Aromatics
Ribisin A
C13H12O5 = 248
J. Org. Chem.    2014, 79 , 2829
P. Lan, M. G. Banwell, A. C. Willis
DOI: 10.1021/jo500210k
CrossRef
 
chiral
racemic
Notes:


Aromatics
Aspergillumarin B
C14H18O4 = 250
Tetrahedron Lett.    2014, 55 , 2921
J. S. Yadav, A. K. Mishra, S. S. Dachavaram, S. G. Kumar, S. Das
DOI: 10.1016/j.tetlet.2014.03.067
CrossRef
 
chiral
racemic
Notes:


Aromatics
Ribisin B
C14H14O5 = 262
J. Org. Chem.    2014, 79 , 2829
P. Lan, M. G. Banwell, A. C. Willis
DOI: 10.1021/jo500210k
CrossRef
 
chiral
racemic
Notes: revised structure


Aromatics
Penicimarin B
C15H20O4 = 264
Tetrahedron Lett.    2014, 55 , 2921
J. S. Yadav, A. K. Mishra, S. S. Dachavaram, S. G. Kumar, S. Das
DOI: 10.1016/j.tetlet.2014.03.067
CrossRef
 
chiral
racemic
Notes:


Aromatics
Ribisin D
C14H14O6 = 278
J. Org. Chem.    2014, 79 , 2829
P. Lan, M. G. Banwell, A. C. Willis
DOI: 10.1021/jo500210k
CrossRef
 
chiral
racemic
Notes:


Aromatics
Clavilactone B
C16H14O5 = 286
Angew. Chem. Int. Ed.    2014, 53 , 4164
L. Lv, B. Shen, Z. Li
DOI: 10.1002/anie.201400326
CrossRef
 
chiral
racemic
Notes:


Aromatics
Clavilactone A
C16H16O5 = 288
Angew. Chem. Int. Ed.    2014, 53 , 4164
L. Lv, B. Shen, Z. Li
DOI: 10.1002/anie.201400326
CrossRef
 
chiral
racemic
Notes:


Aromatics
Clavilactone D
C16H14O6 = 302
Angew. Chem. Int. Ed.    2014, 53 , 4164
L. Lv, B. Shen, Z. Li
DOI: 10.1002/anie.201400326
CrossRef
 
chiral
racemic
Notes: Proposed structure


Aromatics
Cannabinol
C21H26O2 = 310
Adv. Synth. Catal.    2014, 356 , 1337
F. Fan, J. Dong, J. Wang, L. Song, C. Song, J. Chang
DOI: 10.1002/adsc.201301037
CrossRef
 
chiral
racemic
Notes:


Aromatics
Bergenin
C14H16O9 = 328
Chem. Eur. J.    2014, 20 , 4414
K. Parkan, R. Pohl, M. Kotora
DOI: 10.1002/chem.201304304
CrossRef
 
chiral
racemic
Notes:


Aromatics
Zeaenol
C19H24O7 = 364
Eur. J. Org. Chem.    2014, , 2092
Y. Gao, J. Liu, L. Wang, M. Xiao, Y. Du
DOI: 10.1002/ejoc.201301613
CrossRef
 
chiral
racemic
Notes:


Aromatics
Calophione A
C20H16O7 = 368
Eur. J. Org. Chem.    2014, , 2496
R. Worayuthakarn, S. Boonya-udtayan, S. Ruchirawat, N. Thasana
DOI: 10.1002/ejoc.201301722
CrossRef
 
chiral
racemic
Notes:


Aromatics
Cochliomycin A
C22H28O7 = 404
Tetrahedron    2014, 70 , 2616
L. Wang, Y. Gao, J. Liu, C. Cai, Y. Du
DOI: 10.1016/j.tet.2014.03.001
CrossRef
 
chiral
racemic
Notes:


Aromatics
Cochliomycin B
C22H28O7 = 404
Eur. J. Org. Chem.    2014, , 2092
Y. Gao, J. Liu, L. Wang, M. Xiao, Y. Du
DOI: 10.1002/ejoc.201301613
CrossRef
 
chiral
racemic
Notes:


Aromatics
Rubromycin, g-
C26H18O12 = 522
Angew. Chem. Int. Ed.    2014, 53 , 4332
M. Wilsdorf, H.-U. Reissig
DOI: 10.1002/anie.201400315
CrossRef
 
chiral
racemic
Notes:


  63 data found. 1 - 30 listed Next Last   
   
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