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Organic and Biomolecular Chemistry

Volumn 10, Issue 2, 2012, Pages 361-366

A novel D-ring modified taxoid: Synthesis and biological evaluation of a γ-lactone analogue of docetaxel

(5) Gao, Feng a,b Yang, Zhan Kun a Chen, Qiao Hong a Chen, Xiao Guang c Wang, Feng Peng a

a SICHUAN UNIVERSITY (China)

b SICHUAN AGRICULTURAL UNIVERSITY (China)

c INSTITUTE OF MATERIA MEDICA (China)

Author keywords

[No Author keywords available]

Indexed keywords

10-DEACETYLBACCATIN III; BIOLOGICAL EVALUATION; CANCER CELL LINES; DOCETAXEL; HYDROXYL GROUPS; INTRAMOLECULAR ALDOL REACTIONS; MTT ASSAYS; OXETANES; PACLITAXEL; TAXOIDS;

ACETYLATION; CELL CULTURE; CONDENSATION REACTIONS;

SYNTHESIS (CHEMICAL);

ANTINEOPLASTIC AGENT; DOCETAXEL; LACTONE; TAXOID;

ARTICLE; CELL PROLIFERATION; CHEMISTRY; CONFORMATION; DOSE RESPONSE; DRUG EFFECT; DRUG SCREENING; HUMAN; STEREOISOMERISM; STRUCTURE ACTIVITY RELATION; SYNTHESIS; TUMOR CELL LINE;

ANTINEOPLASTIC AGENTS; CELL LINE, TUMOR; CELL PROLIFERATION; DOSE-RESPONSE RELATIONSHIP, DRUG; DRUG SCREENING ASSAYS, ANTITUMOR; HUMANS; LACTONES; MOLECULAR CONFORMATION; STEREOISOMERISM; STRUCTURE-ACTIVITY RELATIONSHIP; TAXOIDS;

EID: 83455201065 PISSN: 14770520 EISSN: None Source Type: Journal
DOI: 10.1039/c1ob06535a Document Type: Article

Times cited : (8)

References (18)

1
- 34447107974
- D. G. I. Kingston Phytochemistry 2007 68 1844
- (2007) Phytochemistry , vol.68 , pp. 1844
- Kingston, D.G.I.¹

2
- 0025871603
- G. Samaranayake N. F. Magri C. Jitrangeri D. G. I. Kingston J. Org. Chem. 1991 56 5114
- (1991) J. Org. Chem. , vol.56 , pp. 5114
- Samaranayake, G.¹ Magri, N.F.² Jitrangeri, C.³ Kingston, D.G.I.⁴

3
- 0033574481
- A. A. L. Gunatilaka F. D. Ramdayal M. H. Sarragiotto D. G. I. Kingston D. L. Sackett E. Hamel J. Org. Chem. 1999 64 2694
- (1999) J. Org. Chem. , vol.64 , pp. 2694
- Gunatilaka, A.A.L.¹ Ramdayal, F.D.² Sarragiotto, M.H.³ Kingston, D.G.I.⁴ Sackett, D.L.⁵ Hamel, E.⁶

4
- 0035958474
- L. Merckle J. Dubois E. Place S. Thoret F. Guéritte D. Guenard C. Poupat A. Ahond P. Potier J. Org. Chem. 2001 66 5058
- (2001) J. Org. Chem. , vol.66 , pp. 5058
- Merckle, L.¹ Dubois, J.² Place, E.³ Thoret, S.⁴ Guéritte, F.⁵ Guenard, D.⁶ Poupat, C.⁷ Ahond, A.⁸ Potier, P.⁹

5
- 0007953052
- R. Marder-Karsenti J. Dubois L. Bricard D. Guénard F. Guéritte-Voegelein J. Org. Chem. 1997 62 6631
- (1997) J. Org. Chem. , vol.62 , pp. 6631
- Marder-Karsenti, R.¹ Dubois, J.² Bricard, L.³ Guénard, D.⁴ Guéritte-Voegelein, F.⁵

6
- 0033581560
- T. C. Boge M. Hepperle D. G. V. Velde C. W. Gunn G. L. Grunewald G. I. Georg Bioorg. Med. Chem. Lett. 1999 9 3041
- (1999) Bioorg. Med. Chem. Lett. , vol.9 , pp. 3041
- Boge, T.C.¹ Hepperle, M.² Velde, D.G.V.³ Gunn, C.W.⁴ Grunewald, G.L.⁵ Georg, G.I.⁶

7
- 0034712232
- M. Wang B. Cornett J. Nettles D. C. Liotta J. P. Snyder J. Org. Chem. 2000 65 1059
- (2000) J. Org. Chem. , vol.65 , pp. 1059
- Wang, M.¹ Cornett, B.² Nettles, J.³ Liotta, D.C.⁴ Snyder, J.P.⁵

8
- 0034728938
- J. Dubois S. Thoret F. Guéritte D. Guénard Tetrahedron Lett. 2000 41 3331
- (2000) Tetrahedron Lett. , vol.41 , pp. 3331
- Dubois, J.¹ Thoret, S.² Guéritte, F.³ Guénard, D.⁴

9
- 10744225655
- L. Barboni G. Giarlo M. Ricciutelli R. Ballini G. I. Georg D. G. VanderVelde R. H. Himes M. Wang A. Lakdawala J. P. Snyder Org. Lett. 2004 6 461
- (2004) Org. Lett. , vol.6 , pp. 461
- Barboni, L.¹ Giarlo, G.² Ricciutelli, M.³ Ballini, R.⁴ Georg, G.I.⁵ Vandervelde, D.G.⁶ Himes, R.H.⁷ Wang, M.⁸ Lakdawala, A.⁹ Snyder, J.P.¹⁰

10
- 0347286692
- V. Deka J. Dubois S. Thoret F. Guéritte D. Guénard Org. Lett. 2003 5 5031
- (2003) Org. Lett. , vol.5 , pp. 5031
- Deka, V.¹ Dubois, J.² Thoret, S.³ Guéritte, F.⁴ Guénard, D.⁵

11
- 33745683548
- S. Thoret F. Guéritte D. Guénard J. Dubois Org. Lett. 2006 8 2301
- (2006) Org. Lett. , vol.8 , pp. 2301
- Thoret, S.¹ Guéritte, F.² Guénard, D.³ Dubois, J.⁴

12
- 0026725902
- P. A. Wender D. B. Rawlins Tetrahedron 1992 48 7033
- (1992) Tetrahedron , vol.48 , pp. 7033
- Wender, P.A.¹ Rawlins, D.B.²

13
- 0028354864
- S.-H. Chen V. Farina J.-M. Wei B. Long C. Fairchild S. W. Mamver J. F. Kadow D. Vyas T. Doyle Bioorg. Med. Chem. Lett. 1994 4 479
- (1994) Bioorg. Med. Chem. Lett. , vol.4 , pp. 479
- Chen, S.-H.¹ Farina, V.² Wei, J.-M.³ Long, B.⁴ Fairchild, C.⁵ Mamver, S.W.⁶ Kadow, J.F.⁷ Vyas, D.⁸ Doyle, T.⁹

14
- 83455254545
- US Patent 5,015,744
- R. A. Holton, US Patent (1991) 5,015,744
- (1991)
- Holton, R.A.¹

15
- 83455231686
- US Patent 5,136,060 also see
- US Patent (1992) 5,136,060
- (1992)

16
- 0027173282
- I. Ojima C. M. Sun M. Zucoo Y. H. Park O. Duclos S. D. Kuduk Tetrahedron Lett. 1993 34 4149
- (1993) Tetrahedron Lett. , vol.34 , pp. 4149
- Ojima, I.¹ Sun, C.M.² Zucoo, M.³ Park, Y.H.⁴ Duclos, O.⁵ Kuduk, S.D.⁶

17
- 0028293455
- A. D. Da Silva A. S. Machado C. Tempête Eur. J. Med. Chem. 1994 29 149
- (1994) Eur. J. Med. Chem. , vol.29 , pp. 149
- Da Silva, A.D.¹ MacHado, A.S.² Tempête, C.³

18
- 0035906452
- L. Barboni A. Datta D. Dutta G. I. Georg D. V. V. Velde R. H. Himes M. Wang J. P. Snyder J. Org. Chem. 2001 66 3321
- (2001) J. Org. Chem. , vol.66 , pp. 3321
- Barboni, L.¹ Datta, A.² Dutta, D.³ Georg, G.I.⁴ Velde, D.V.V.⁵ Himes, R.H.⁶ Wang, M.⁷ Snyder, J.P.⁸

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