SCOPUS 정보 검색 플랫폼 - 논문 보기

메뉴 건너뛰기

Chemical Communications

Volumn , Issue 5, 2009, Pages 592-594

A thermal 6π electrocyclization strategy towards taiwaniaquinoids. First enantiospecific synthesis of (-)-taiwaniaquinone G

(9) Alvarez Manzaneda, Enrique a Chahboun, Rachid a Cabrera, Eduardo a Alvarez, Esteban a Haidour, Ali a Ramos, Jose Miguel a Alvarez Manzaneda, Ramón b Hmamouchi, Mohammed c Es Samti, Hakima c

a UNIVERSITY OF GRANADA (Spain)

b UNIVERSITY OF ALMERÍA (Spain)

c MOHAMMED V UNIVERSITY (Morocco)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 58649118388 PISSN: 13597345 EISSN: None Source Type: Journal
DOI: 10.1039/b816812a Document Type: Article

Times cited : (42)

References (24)

1
- 0028850966
- W. Lin J. Fang Y. Chang Phytochemistry 1995 40 871
- (1995) Phytochemistry , vol.40 , pp. 871
- Lin, W.¹ Fang, J.² Chang, Y.³

2
- 0030207685
- W. Lin J. Fang Y. Cheng Phytochemistry 1996 42 1657
- (1996) Phytochemistry , vol.42 , pp. 1657
- Lin, W.¹ Fang, J.² Cheng, Y.³

3
- 3142769317
- C. Chang S. Chien S. Lee Y. Kuo Chem. Pharm. 2003 51 1420
- (2003) Chem. Pharm. , vol.51 , pp. 1420
- Chang, C.¹ Chien, S.² Lee, S.³ Kuo, Y.⁴

4
- 13544276907
- C.-I. Chang J.-Y. Chang C.-C. Kuo W.-Y. Pan Y.-H. Kuo Planta Med. 2005 71 72
- (2005) Planta Med. , vol.71 , pp. 72
- Chang, C.-I.¹ Chang, J.-Y.² Kuo, C.-C.³ Pan, W.-Y.⁴ Kuo, Y.-H.⁵

5
- 0033609869
- H. Ohtsu M. Iwamoto U. Ohishi S. Matsunaga R. Tanaka Tetrahedron Lett. 1999 40 6419
- (1999) Tetrahedron Lett. , vol.40 , pp. 6419
- Ohtsu, H.¹ Iwamoto, M.² Ohishi, U.³ Matsunaga, S.⁴ Tanaka, R.⁵

6
- 0345059823
- K. Kawazoe M. Yamamoto Y. Takaishi G. Honda T. Fujita E. Sezik Phytochemistry 1999 50 493
- (1999) Phytochemistry , vol.50 , pp. 493
- Kawazoe, K.¹ Yamamoto, M.² Takaishi, Y.³ Honda, G.⁴ Fujita, T.⁵ Sezik, E.⁶

7
- 0034939302
- M. Iwamoto H. Ohtsu H. Tokuda H. Nishino S. Matsunaga R. Tanaka Bioorg. Med. Chem. 2001 9 1911
- (2001) Bioorg. Med. Chem. , vol.9 , pp. 1911
- Iwamoto, M.¹ Ohtsu, H.² Tokuda, H.³ Nishino, H.⁴ Matsunaga, S.⁵ Tanaka, R.⁶

8
- 0036675140
- T. Minami M. Iwamoto H. Ohtsu H. Ohishi R. Tanaka A. Yoshitake Planta Med. 2002 68 742
- (2002) Planta Med. , vol.68 , pp. 742
- Minami, T.¹ Iwamoto, M.² Ohtsu, H.³ Ohishi, H.⁴ Tanaka, R.⁵ Yoshitake, A.⁶

9
- 1942534025
- J. Hanson Nat. Prod. Rep. 2004 21 312
- (2004) Nat. Prod. Rep. , vol.21 , pp. 312
- Hanson, J.¹

10
- 33745417849
- R. M. Mc Fadden B. M. Stoltz J. Am. Chem. Soc. 2006 128 7738
- (2006) J. Am. Chem. Soc. , vol.128 , pp. 7738
- Mc Fadden, R.M.¹ Stoltz, B.M.²

11
- 25444492377
- E. Fillion D. Fishlock J. Am. Chem. Soc. 2005 127 13144
- (2005) J. Am. Chem. Soc. , vol.127 , pp. 13144
- Fillion, E.¹ Fishlock, D.²

12
- 39149137187
- S. Li P. Chiu Tetrahedron Lett. 2008 49 1741
- (2008) Tetrahedron Lett. , vol.49 , pp. 1741
- Li, S.¹ Chiu, P.²

13
- 33748089380
- G. Liang Y. Xu I. B. Sciple D. Trauner J. Am. Chem. Soc. 2006 126 11022
- (2006) J. Am. Chem. Soc. , vol.126 , pp. 11022
- Liang, G.¹ Xu, Y.² Sciple, I.B.³ Trauner, D.⁴

14
- 33645533634
- L. Planas M. Mogi H. Takita T. Ajimoto M. Node J. Org. Chem. 2006 71 2896
- (2006) J. Org. Chem. , vol.71 , pp. 2896
- Planas, L.¹ Mogi, M.² Takita, H.³ Ajimoto, T.⁴ Node, M.⁵

15
- 0242712444
- M. Banerjee R. Mukhopadhyay B. Achari A. K. Banerjee Org. Lett. 2003 5 3931
- (2003) Org. Lett. , vol.5 , pp. 3931
- Banerjee, M.¹ Mukhopadhyay, R.² Achari, B.³ Banerjee, A.K.⁴

16
- 33645499302
- M. Banerjee R. Mukhopadhyay B. Achari A. K. Banerjee J. Org. Chem. 2006 71 2787
- (2006) J. Org. Chem. , vol.71 , pp. 2787
- Banerjee, M.¹ Mukhopadhyay, R.² Achari, B.³ Banerjee, A.K.⁴

17
- 48849104990
- S. Tang Y. Xu J. He J. Zheng X. Pan X. She Org. Lett. 2008 10 1855
- (2008) Org. Lett. , vol.10 , pp. 1855
- Tang, S.¹ Xu, Y.² He, J.³ Zheng, J.⁴ Pan, X.⁵ She, X.⁶

18
- 2342471814
- and references cited therein
- E. J. Alvarez-Manzaneda R. Chahboun E. Cabrera Torres E. Alvarez R. Alvarez-Manzaneda A. Haidour J. M. Ramos Tetrahedron Lett. 2004 45 4453
- (2004) Tetrahedron Lett. , vol.45 , pp. 4453
- Alvarez-Manzaneda, E.J.¹ Chahboun, R.² Cabrera Torres, E.³ Alvarez, E.⁴ Alvarez-Manzaneda, R.⁵ Haidour, A.⁶ Ramos, J.M.⁷

19
- 0029889362
- Synthesis of compound 14 has also been reported by Hagiwara et al. These authors prepared this homoallylic iodide from a Wieland-Miescher ketone analogue, after an 11-step sequence (21% overall yield). See:
- H. Tanimoto T. Oritani Tetrahedron: Asymmetry 1996 7 1695
- (1996) Tetrahedron: Asymmetry , vol.7 , pp. 1695
- Tanimoto, H.¹ Oritani, T.²

20
- 1042298791
- H. Hagiwara F. Takeuchi M. Nozawa T. Hoshi T. Suzuki Tetrahedron 2004 60 1983
- (2004) Tetrahedron , vol.60 , pp. 1983
- Hagiwara, H.¹ Takeuchi, F.² Nozawa, M.³ Hoshi, T.⁴ Suzuki, T.⁵

21
- 33748661727
- H. Hagiwara H. Nagatomo S. Kazayama H. Sakai T. Hoshi T. Suzuki M. Ando J. Chem. Soc., Perkin Trans. 1 1999 457
- (1999) J. Chem. Soc., Perkin Trans. 1 , pp. 457
- Hagiwara, H.¹ Nagatomo, H.² Kazayama, S.³ Sakai, H.⁴ Hoshi, T.⁵ Suzuki, T.⁶ Ando, M.⁷

22
- 33845279247
- Ozonolysis of compound 14 to give diketone 18 has also been accomplished by Hagiwara's group (ref. 14a). However, these authors reported low yields for this transformation, probably due to the small quantity of starting material they utilized
- H. Hagiwara H. Uda J. Org. Chem. 1988 53 2308
- (1988) J. Org. Chem. , vol.53 , pp. 2308
- Hagiwara, H.¹ Uda, H.²

23
- 0038102356
- G. A. Kraus I. Kim J. Org. Chem. 2003 68 4517
- (2003) J. Org. Chem. , vol.68 , pp. 4517
- Kraus, G.A.¹ Kim, I.²

24
- 0037164654
- G. A. Kraus N. Zhang Tetrahedron Lett. 2002 43 9597
- (2002) Tetrahedron Lett. , vol.43 , pp. 9597
- Kraus, G.A.¹ Zhang, N.²

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.