-
1
-
-
0001623106
-
-
Atta-ur-Rahman (Ed.); Elsevier Science: Amsterdam
-
Nakano, T. In Studies in Natural Products Chemistry; Atta-ur-Rahman (Ed.); Elsevier Science: Amsterdam, 1989; vol. 4, pp. 403-429, and references cited therein.
-
(1989)
Studies in Natural Products Chemistry
, vol.4
, pp. 403-429
-
-
Nakano, T.1
-
2
-
-
0030087689
-
Antimicrobial abietane diterpenoids from Plectranthus elegans
-
(a) Dellar, J. E.; Cole, M. D.; Waterman, P. G. Antimicrobial abietane diterpenoids from Plectranthus elegans. Phytochemistry 1996, 41, 735-738;
-
(1996)
Phytochemistry
, vol.41
, pp. 735-738
-
-
Dellar, J.E.1
Cole, M.D.2
Waterman, P.G.3
-
3
-
-
0029138724
-
An antimicrobial abietane from the root of Plectranthus hereroensis
-
(b) Batista, O.; Simoes, F.; Duarte, A.; Valdeira, M. L.; de la Torre, M.; Rodriguez, B. An antimicrobial abietane from the root of Plectranthus hereroensis. Phytochemistry 1995, 38, 167-169;
-
(1995)
Phytochemistry
, vol.38
, pp. 67-169
-
-
Batista, O.1
Simoes, F.2
Duarte, A.3
Valdeira, M.L.4
De La Torre, M.5
Rodriguez, B.6
-
4
-
-
85007932316
-
Constituents of spices of the family Labiatae, part III: Two antioxidative diterpenes from rosemary (Rosmarinus officinalis L.) and a revised structure for rosmanol
-
(c) Nakatani, N.; Inatani, R. Constituents of spices of the family Labiatae, part III: Two antioxidative diterpenes from rosemary (Rosmarinus officinalis L.) and a revised structure for rosmanol. Agric. Biol. Chem. 1984, 48, 2081;
-
(1984)
Agric. Biol. Chem.
, vol.48
, pp. 2081
-
-
Nakatani, N.1
Inatani, R.2
-
5
-
-
0001584094
-
Antimalarial compounds from Hoslundia opposita
-
(d) Achenbach, H.; Waibel, R.; Nkunya, M. H. H.; Weenen, H. Antimalarial compounds from Hoslundia opposita. Phytochemistry 1992, 31, 3781-3784;
-
(1992)
Phytochemistry
, vol.31
, pp. 3781-3784
-
-
Achenbach, H.1
Waibel, R.2
Nkunya, M.H.H.3
Weenen, H.4
-
6
-
-
0031080991
-
Cytotoxic abietane diterpenoids from Caryopteris incana
-
DOI 10.1016/S0031-9422(96)00609-7, PII S0031942296006097
-
(e) Gao, J.; Han, G. Cytotoxic abietane diterpenoids from Caryopteris incana. Phytochemistry 1997, 44, 759-761. (Pubitemid 27073888)
-
(1997)
Phytochemistry
, vol.44
, Issue.4
, pp. 759-761
-
-
Gao, J.1
Han, G.2
-
7
-
-
0034072640
-
Six podocarpane-type trinorditerpenes from the bark of Taiwania cryptomerioides
-
Kuo, Y.-H.; Chang, Ch.-I.; Lee, Ch.-K. Six podocarpane-type trinorditerpenes from the bark of Taiwania cryptomerioides. Chem. Pharm. Bull. 2000, 48, 597-599. (Pubitemid 30321979)
-
(2000)
Chemical and Pharmaceutical Bulletin
, vol.48
, Issue.5
, pp. 597-599
-
-
Kuo, Y.-H.1
Chang, C.-I.2
Lee, C.-K.3
-
8
-
-
30344477665
-
Isolation, synthesis, and anti-tumor activities of a novel class of podocarpic diterpenes
-
DOI 10.1016/j.bmcl.2005.11.023, PII S0960894X05014459
-
Xiong, Y.; Wang, K.; Pan, Y.; Sun, H.; Tu, J. Isolation, synthesis, and anti-tumor activities of a novel class of podocarpic diterpenes. Bioorg. Med. Chem. Lett. 2006, 16, 786-789. (Pubitemid 43059822)
-
(2006)
Bioorganic and Medicinal Chemistry Letters
, vol.16
, Issue.4
, pp. 786-789
-
-
Xiong, Y.1
Wang, K.2
Pan, Y.3
Sun, H.4
Tu, J.5
-
9
-
-
0001140189
-
Polyene cyclizations
-
B. M. Trost and I. Fleming (Eds.); Pergamon Press: Oxford
-
(a) Sutherland, J. K. Polyene cyclizations. In Comprehensive Organic Synthesis; B. M. Trost and I. Fleming (Eds.); Pergamon Press: Oxford, 1991; vol. 3, pp. 341-377;
-
(1991)
Comprehensive Organic Synthesis
, vol.3
, pp. 341-377
-
-
Sutherland, J.K.1
-
10
-
-
0027968750
-
2: An unusually efficient method for the direct, stereospecific synthesis of polycyclic intermediates via cationic initiation at non-functionalized 3 alkenes: An application to the total synthesis of (-)-taxodione
-
2: An unusually efficient method for the direct, stereospecific synthesis of polycyclic intermediates via cationic initiation at non-functionalized 3 alkenes: An application to the total synthesis of (-)-taxodione. Tetrahedron 1994, 50, 9229-9254;
-
(1994)
Tetrahedron
, vol.50
, pp. 9229-9254
-
-
Harring, S.R.1
Livinghouse, T.2
-
11
-
-
0013172046
-
Approach to the synthesis of candelabrone and synthesis of 3,7-diketo-12-hydroxyabieta- 8,11,13-triene
-
(c) Burnell, R. H.; Caron, S. Approach to the synthesis of candelabrone and synthesis of 3,7-diketo-12-hydroxyabieta- 8,11,13-triene. Can. J. Chem. 1992, 70, 1446-1454;
-
(1992)
Can. J. Chem.
, vol.70
, pp. 1446-1454
-
-
Burnell, R.H.1
Caron, S.2
-
12
-
-
0034699201
-
Synthesis of (+)- and (-)-ferruginol via asymmetric cyclization of a polyene
-
(d) Tada, M.; Nishiiri, S.; Zhixiang, Y.; Imai, Y.; Tajima, S.; Okazaki, N.; Kitano, Y.; Chiba, K. Synthesis of (+)- and (-)- ferruginol via asymmetric cyclization of a polyene. J. Chem. Soc., Perkin Trans. 1 2000, 2657-2664; (Pubitemid 35290692)
-
(2000)
Journal of the Chemical Society, Perkin Transactions 1
, Issue.16
, pp. 2657-2664
-
-
Tada, M.1
Nishiiri, S.2
Zhixiang, Y.3
Imai, Y.4
Tajima, S.5
Okazaki, N.6
Kitano, Y.7
Chiba, K.8
-
13
-
-
0035925119
-
Enantioselective biomimetic cyclization of homo(polyprenyl)arenes. A new entry to (+)-podpcarpa-8,11,13-triene diterpenoids and (-)-tetracyclic polyprenoid of sedimentary origin [4]
-
DOI 10.1021/ja003541x
-
(e) Ishihara, K.; Ishibashi, H.; Yamamoto, H. Enantioselective biomimetic cyclization of homo(polyprenyl)arenes: A new entry to (+)-podpcarpa-8,11,13- triene diterpenoids and (-)-tetracyclic polyprenoid of sedimentary origin. J. Am. Chem. Soc. 2001, 123, 1505-1506; (Pubitemid 32167345)
-
(2001)
Journal of the American Chemical Society
, vol.123
, Issue.7
, pp. 1505-1506
-
-
Ishihara, K.1
Ishibashi, H.2
Yamamoto, H.3
-
14
-
-
0037051649
-
Enantio- and diastereoselective stepwise cyclization of polyprenoids induced by chiral and achiral LBAs. A new entry to (-)-ambrox, (+)-podocarpa-8,11,13-triene diterpenoids, and (-)-tetracyclic polyprenoid of sedimentary origin
-
DOI 10.1021/ja0124865
-
(f) Ishihara, K.; Ishibashi, H.; Yamamoto, H. Enantio- and diastereoselective stepwise cyclization of polyprenoids induced by chiral and achiral LBAs: A new entry to (-)-ambrox, (+)-podocarpa-8,11,13-triene diterpenoids, and (-)-tetracyclic polyprenoid of sedimentary origin. J. Am. Chem. Soc. 2002, 124, 3647-3655; (Pubitemid 34407888)
-
(2002)
Journal of the American Chemical Society
, vol.124
, Issue.14
, pp. 3647-3655
-
-
Ishihara, K.1
Ishibashi, H.2
Yamamoto, H.3
-
15
-
-
0030753216
-
Use of conjugated dienones in cyclialkylations: Total syntheses of arucadiol, 1,2-didehydromiltirone, (-)-hinokione, (-)-nimbidiol, sageone, and miltirone
-
DOI 10.1021/jo970570q
-
(g) Majetich, G.; Liu, S.; Fang, J.; Siesel, D.; Zhang, Y. Use of conjugated dienones in cycloalkylations: Total syntheses of arucadiol, 1,2-didehydromiltirone, (-)-hinokione, (-)-nimbidiol, sageone, and miltirone. J. Org. Chem. 1997, 62, 6928-6951. (Pubitemid 27443750)
-
(1997)
Journal of Organic Chemistry
, vol.62
, Issue.20
, pp. 6928-6951
-
-
Majetich, G.1
Liu, S.2
Fang, J.3
Siesel, D.4
Zhang, Y.5
-
16
-
-
2542616938
-
Synthesis of drimanic sesquiterpenes (+)-valdiviolide (+)-12a-hydroxyisodrimenin and (+)-winterin
-
(a) Nakano, T.; Villamizar, J.; Maillo, M. A. Synthesis of drimanic sesquiterpenes, (+)-valdiviolide, (+)-12a-hydroxyisodrimenin, and (+)-winterin. J. Chem. Res. Synop. 1998, 560-561;
-
(1998)
J. Chem. Res. Synop.
, pp. 560-561
-
-
Nakano, T.1
Villamizar, J.2
Maillo, M.A.3
-
18
-
-
0029058569
-
A facile access to optically active ring C aromatic diterpene derivatives: Highly efficient synthesis of (+)-12-methyl-7-oxopodocarpa-8,11,13- triene-13-carboxylic acid and (+)-13-methyl-7-oxopodocarpa-8,11,13-triene-12- carboxylic acid from manool
-
(a) Nakano, T.; Alonso, R.; Maillo, M. A.; Martin, A.; Nunez, R. A. A facile access to optically active ring C aromatic diterpene derivatives: Highly efficient synthesis of (+)-12-methyl-7-oxopodocarpa-8,11,13-triene-13-carboxylic acid and (+)-13-methyl-7-oxopodocarpa-8,11,13-triene-12-carboxylic acid from manool. Tetrahedron Lett. 1995, 36, 3801-3804;
-
(1995)
Tetrahedron Lett.
, vol.36
, pp. 3801-3804
-
-
Nakano, T.1
Alonso, R.2
Maillo, M.A.3
Martin, A.4
Nunez, R.A.5
-
19
-
-
0013172047
-
Facile access to optically active ring C aromatic diterpene derivatives from manool. Highly efficient syntheses of (+)-12-methyl-7-oxo-podocarpa-8,11, 13-triene-13-carboxylic acid, (+)-13-methyl-7-oxopodocarpa-8,11,13-triene-12- carboxylic acid and (+)-nimbiol
-
(b) Nakano, T.; Alonso, R.; Maillo, M. A.; Martin, A.; Nunez, R. A. Facile access to optically active ring C aromatic diterpene derivatives from manool: Highly efficient syntheses of (+)-12-methyl-7-oxopodocarpa-8,11,13- triene-13-carboxylic acid, (+)-13-methyl-7-oxopodocarpa-8,11,13-triene-12- carboxylic acid, and (+)-nimbiol. J. Chem. Soc., Perkin Trans. 1, 1998, 1423-1426. (Pubitemid 128757874)
-
(1998)
Journal of the Chemical Society - Perkin Transactions 1
, Issue.8
, pp. 1423-1426
-
-
Nakano, T.1
Alonso, R.2
Maillo, M.A.3
Martin, A.4
Nunez, R.A.5
-
20
-
-
0347026018
-
Facile Access to Optically Active Labdane-Type Diterpenes from (+)-Manool. Synthesis of (+)-Coronarin E, (+)-15,16-Epoxy-8(17),13(16),14- labdatriene, and (+)-Labda-8(17),13(Z)-diene-15,16-diol
-
DOI 10.1021/np030166o
-
(a) Villamizar, J.; Fuentes, J.; Salazar, F.; Tropper, E.; Alonso, R. Facile access to optically active labdane-type diterpenes from (+)-manool: Synthesis of (+)-coronarin E, (+)-15,16-epoxy-8(17),13(16),14-labdatriene, and (+)-labda-8(17),13(Z)-diene-15,16-diol. J. Nat. Prod. 2003, 66, 1623-1627; (Pubitemid 38036720)
-
(2003)
Journal of Natural Products
, vol.66
, Issue.12
, pp. 1623-1627
-
-
Villamizar, J.1
Fuentes, J.2
Salazar, F.3
Tropper, E.4
Alonso, R.5
-
21
-
-
0036697733
-
Highly efficient synthesis of optically active sesquiterpene hydroquinone (+)-zonarol and sesquiterpene quinone (+)-zonarone
-
(b) Villamizar, J.; Orcajo, A. L.; Fuentes, J.; Tropper, E.; Alonso, R. Highly efficient synthesis of optically active sesquiterpene hydroquinone (+)-zonarol and sesquiterpene quinone (+)-zonarone. J. Chem. Res. Synop. 2002, 395-397;
-
(2002)
J. Chem. Res. Synop.
, pp. 395-397
-
-
Villamizar, J.1
Orcajo, A.L.2
Fuentes, J.3
Tropper, E.4
Alonso, R.5
-
22
-
-
34547768082
-
Facile access to labdane-type diterpenes: Synthesis of coronarin C zerumin B labda-8(17),13(14)-dien-15,16-olide, and derivatives from (+)-manool
-
(c) Villamizar, J. E.; Juncosa, J.; Pittelaud, J.; Hernandez, M.; Canudas, N.; Tropper, E.; Salazar, F.; Fuentes, J. Facile access to labdane-type diterpenes: Synthesis of coronarin C, zerumin B, labda-8(17),13(14)-dien-15,16- olide, and derivatives from (+)-manool. J. Chem. Res. 2007, 342-346.
-
(2007)
J. Chem. Res.
, pp. 342-346
-
-
Villamizar, J.E.1
Juncosa, J.2
Pittelaud, J.3
Hernandez, M.4
Canudas, N.5
Tropper, E.6
Salazar, F.7
Fuentes, J.8
-
23
-
-
0037463518
-
First formal synthesis of (+)-nimbidiol. Synthesis, X-ray structure and anticancer activity of a novel ring C aromatic diterpene: Dimethyl (+)-podocarpa-8,11,13-triene-12,13-dicarboxylate
-
DOI 10.1016/S0040-4039(03)00105-9, PII S0040403903001059
-
Zambrano, J. L.; Rosales, V.; Nakano, T. First formal synthesis of (+)-nimbidiol: Synthesis, x-ray structure, and anticancer activity of a novel ring C aromatic diterpene: Dimethyl (+)-podocarpa-8,11,13-triene-12,13- dicarboxylate. Tetrahedron Lett. 2003, 44, 1859-1862. (Pubitemid 36183418)
-
(2003)
Tetrahedron Letters
, vol.44
, Issue.9
, pp. 1859-1862
-
-
Zambrano, J.L.1
Rosales, V.2
Nakano, T.3
-
24
-
-
36048972000
-
Novel synthetic strategy toward abietane and podocarpane-type diterpenes from (-)-sclareol: synthesis of the antitumor (+)-7-deoxynimbidiol
-
DOI 10.1016/j.tetlet.2007.10.080, PII S0040403907020886
-
Alvarez-Manzaneda, E.; Chahboun, R.; Cabrera, E.; Alvarez, E.; Alvarez-Manzaneda, R.; Hmamouchi, M.; Es-Samti, H. Novel synthetic strategy toward abietane and podocarpane-type diterpenes from (-)-sclareol: Synthesis of the antitumor (+)-7-deoxynimbidiol. Tetrahedron Lett. 2007, 48, 8930-8934. (Pubitemid 350090008)
-
(2007)
Tetrahedron Letters
, vol.48
, Issue.50
, pp. 8930-8934
-
-
Alvarez-Manzaneda, E.1
Chahboun, R.2
Cabrera, E.3
Alvarez, E.4
Alvarez-Manzaneda, R.5
Hmamouchi, M.6
Es-Samti, H.7
-
25
-
-
33744471124
-
A new route toward 7-oxo-13-hydroxy-8,11,13-podocarpatrienes from labdane diterpenes
-
DOI 10.1021/np0502847
-
Alvarez-Manzaneda Roldan, E.; Santiago, J. L. R.; Chahboun, R. A new route toward 7-oxo-13-hydroxy-8,11,13-podocarpatrienes from labdane diterpenes. J. Nat. Prod. 2006, 69, 563-566. (Pubitemid 43798102)
-
(2006)
Journal of Natural Products
, vol.69
, Issue.4
, pp. 563-566
-
-
Alvarez-Manzaneda Roldan, E.1
Romera Santiago, J.L.2
Chahboun, R.3
-
26
-
-
77958068889
-
Total synthesis of (-)-jolkinolide E, the enantiomer of the natural substance
-
Nakano, T.; Maillo, M. A. Total synthesis of (-)-jolkinolide E, the enantiomer of the natural substance. J. Chem. Res. 1985, 268-269.
-
(1985)
J. Chem. Res.
, pp. 268-269
-
-
Nakano, T.1
Maillo, M.A.2
-
27
-
-
0028081311
-
Novel diastereoselective routes for the synthesis of the ambergris ketals
-
DOI 10.1016/S0040-4039(00)78512-1
-
do Ceu Costa, M.; Tavares, R.; Motherwell, W. B.; Joao, M.; Curto, M. Novel diastereoselective routes for the synthesis of the ambergris ketals. Tetrahedron Lett. 1994, 35, 8839-8842. (Pubitemid 24347894)
-
(1994)
Tetrahedron Letters
, vol.35
, Issue.47
, pp. 8839-8842
-
-
Do Ceu Costa, M.1
Tavares, R.2
Motherwell, W.B.3
Curto, M.J.M.4
-
28
-
-
0023035795
-
Structures of agelasines, diterpenes having a 9-methyladeninium chromophore isolated from the Okinawan marine sponge Agelas nakamurai Hoshino?
-
DOI 10.1246/bcsj.59.2495
-
Wu, H.; Nakamura, H.; Kobayashi, J.; Kobayashi, M.; Ohizumi, Y.; Hirata, Y. Physiologically active marine natural products from Porifera, XII: Structures of agelasines, diterpenes having a 9-methyladeninium chromophore isolated from the Okinawan marine sponge Agelas nakamurai Hoshino. Bull. Chem. Soc. Jpn. 1986, 59, 2495-2504. (Pubitemid 17198247)
-
(1986)
Bulletin of the Chemical Society of Japan
, vol.59
, Issue.8
, pp. 2495-2504
-
-
Wu, H.1
Nakamura, H.2
Kobayashi, J.3
-
29
-
-
37549047192
-
Chemoenzymatic synthesis of (+)-totarol, (+)-podototarin, (+)-sempervirol, and (+)-jolkinolides e and D
-
Miyake, T.; Kigoshi, H.; Akita, H. Chemoenzymatic synthesis of (+)-totarol, (+)-podototarin, (+)-sempervirol, and (+)-jolkinolides E and D. Tetrahedron: Asymmetry 2007, 18, 2915-2922.
-
(2007)
Tetrahedron: Asymmetry
, vol.18
, pp. 2915-2922
-
-
Miyake, T.1
Kigoshi, H.2
Akita, H.3
-
30
-
-
44349128492
-
Manganese(III) acetate: A versatile reagent in organic chemistry
-
Demir, A. S.; Emrullahoglu, M. Manganese(III) acetate: A versatile reagent in organic chemistry. Curr. Org. Synth. 2007, 4( 3), 321-351.
-
(2007)
Curr. Org. Synth.
, vol.4
, Issue.3
, pp. 321-351
-
-
Demir, A.S.1
Emrullahoglu, M.2
|