SCOPUS 정보 검색 플랫폼

Tetrahedron

Volumn 66, Issue 41, 2010, Pages 8210-8213

Efficient synthesis of heterophosphole-2-sulfides by solvent-free microwave reaction

(3) Seijas, Julio A a Vázquez Tato, M Pilar a Crecente Campo, José a

a UNIVERSITY OF SANTIAGO DE COMPOSTELA (Spain)

Author keywords

Heteophosphole 2 sulfides; Lawesson's reagent; Microwave reactions; Solvent free

Indexed keywords

AMINOPHENOL DERIVATIVE; BENZODIAZAPHOSPHOLE 2 SULFIDE; BENZODIOXAPHOSPHOLE 2 SULFIDE; BENZOTHIAZAPHOSPHOLE 2 SULFIDE; BENZOXAZAPHOSPHOLE 2 SULFIDE; CATECHOL DERIVATIVE; PHENYLENEDIAMINE DERIVATIVE; PHOSPHOLE DERIVATIVE; REAGENT; SULFIDE; THIOPHENOL DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL REACTION; CHEMICAL STRUCTURE; MICROWAVE RADIATION; PRIORITY JOURNAL; QUANTUM YIELD; REACTION ANALYSIS; REACTION TIME; STOICHIOMETRY; SYNTHESIS;

EID: 77956615970 PISSN: 00404020 EISSN: None Source Type: Journal
DOI: 10.1016/j.tet.2010.08.011 Document Type: Article

Times cited : (8)

References (25)

1
- 0001401183
- E. Breuer F.R. Hartley, The Chemistry of Organophosphorus Compounds Vol. 4 1996 Wiley New York, NY 653 729
- (1996) The Chemistry of Organophosphorus Compounds , vol.4 , pp. 653-729
- Breuer, E.¹

2
- 0000618403
- T.K. Prakasha, O.R. Day, and R.R. Holmes J. Am. Chem. Soc. 116 1994 8095 8104
- (1994) J. Am. Chem. Soc. , vol.116 , pp. 8095-8104
- Prakasha, T.K.¹ Day, O.R.² Holmes, R.R.³

3
- 77956618546
- C. Fest, K.J. Schmidt, Springer Berlin
- C. Fest, K.J. Schmidt, The Chemistry of Organophosphorus Pesticides Vol. 82 1973 Springer Berlin 12
- (1973) The Chemistry of Organophosphorus Pesticides , vol.82 , pp. 12

4
- 0017132677
- M.S. Bhatia, and P. Jit Experientia 32 1976 1111
- (1976) Experientia , vol.32 , pp. 1111
- Bhatia, M.S.¹ Jit, P.²

5
- 34548048787
- P.N. Manne, S.D. Deshmukh, N.G.V. Rao, H.G. Dodale, S.N. Tikar, and S.A. Nimbalkar Pestology 34 2000 65 67
- (2000) Pestology , vol.34 , pp. 65-67
- Manne, P.N.¹ Deshmukh, S.D.² Rao, N.G.V.³ Dodale, H.G.⁴ Tikar, S.N.⁵ Nimbalkar, S.A.⁶

6
- 0014662797
- D. Hendlin, E.O. Stapley, M. Jackson, H. Wallick, A.K. Miller, F.J. Wolf, T.W. Miller, L. Chaiet, F.M. Kahan, E.L. Foltz, H.B. Woodruff, J.M. Mata, S. Hernandez, and S. Mochales Science 166 1969 122 123
- (1969) Science , vol.166 , pp. 122-123
- Hendlin, D.¹ Stapley, E.O.² Jackson, M.³ Wallick, H.⁴ Miller, A.K.⁵ Wolf, F.J.⁶ Miller, T.W.⁷ Chaiet, L.⁸ Kahan, F.M.⁹ Foltz, E.L.¹⁰ Woodruff, H.B.¹¹ Mata, J.M.¹² Hernandez, S.¹³ Mochales, S.¹⁴

7
- 0036499440
- A.M. Polozov, and S.E. Cremer J. Organomet. Chem. 646 2002 153 160
- (2002) J. Organomet. Chem. , vol.646 , pp. 153-160
- Polozov, A.M.¹ Cremer, S.E.²

8
- 0003064655
- S.L. Deng, and R.Y. Chen Chinese J. Synth. Chem. 9 2001 122 126
- (2001) Chinese J. Synth. Chem. , vol.9 , pp. 122-126
- Deng, S.L.¹ Chen, R.Y.²

9
- 0345754995
- S.L. Deng, R.Y. Chen, and X.F. Yang Chem. J. Chinese Univ. 21 2000 1679 1683
- (2000) Chem. J. Chinese Univ. , vol.21 , pp. 1679-1683
- Deng, S.L.¹ Chen, R.Y.² Yang, X.F.³

10
- 0012557735
- S.L. Deng, R.Y. Chen, and X.F. Yang Chinese J. Appl. Chem. 18 2001 647 650
- (2001) Chinese J. Appl. Chem. , vol.18 , pp. 647-650
- Deng, S.L.¹ Chen, R.Y.² Yang, X.F.³

11
- 0033693125
- L.N. Rao, V.K. Reddy, and C.D. Reddy Heteroat. Chem. 11 2000 323 328
- (2000) Heteroat. Chem. , vol.11 , pp. 323-328
- Rao, L.N.¹ Reddy, V.K.² Reddy, C.D.³

12
- 0029928536
- I. Neda, C. Melnicky, A. Vollbrecht, and R. Schmutzler Synthesis 1996 473 474
- (1996) Synthesis , pp. 473-474
- Neda, I.¹ Melnicky, C.² Vollbrecht, A.³ Schmutzler, R.⁴

13
- 0001332293
- T. Viljanen, P. Taehtinen, K. Pihlaja, and F. Fueloep J. Org. Chem. 63 1998 618 627
- (1998) J. Org. Chem. , vol.63 , pp. 618-627
- Viljanen, T.¹ Taehtinen, P.² Pihlaja, K.³ Fueloep, F.⁴

14
- 0347644772
- J.M. Huang, and R.Y. Chen Chem. J. Chinese Univ. 21 2000 1510 1514
- (2000) Chem. J. Chinese Univ. , vol.21 , pp. 1510-1514
- Huang, J.M.¹ Chen, R.Y.²

15
- 0141483364
- M. Jesberger, T.P. Davis, and L. Barner Synthesis 2003 1929 1958
- (2003) Synthesis , pp. 1929-1958
- Jesberger, M.¹ Davis, T.P.² Barner, L.³

16
- 84859518431
- S. Xiao-Qing, L. Hong-Lei, Z. Hong-Yun, Z. Hong-Quan, M. Hong-Yan, W. Qing-An, Z. Yu, and H. Hong-Wei Chinese J. Struct. Chem. 10 2005 1211 1216
- (2005) Chinese J. Struct. Chem. , vol.10 , pp. 1211-1216
- Xiao-Qing, S.¹ Hong-Lei, L.² Hong-Yun, Z.³ Hong-Quan, Z.⁴ Hong-Yan, M.⁵ Qing-An, W.⁶ Yu, Z.⁷ Hong-Wei, H.⁸

17
- 0002077718
- R. Shabana, L.S. Boulos, and Y.M. Shaker Heteroat. Chem. 10 1999 25 30
- (1999) Heteroat. Chem. , vol.10 , pp. 25-30
- Shabana, R.¹ Boulos, L.S.² Shaker, Y.M.³

18
- 37549044693
- G.S. Prasad, B.H. Babu, C.D. Reddy, C.N. Raju, and C.S. Reddy Synth. Commun. 38 2008 85 91
- (2008) Synth. Commun. , vol.38 , pp. 85-91
- Prasad, G.S.¹ Babu, B.H.² Reddy, C.D.³ Raju, C.N.⁴ Reddy, C.S.⁵

19
- 0027998788
- R. Shabana, F.H. Osman, and S.S. Atrees Tetrahedron 50 1994 6975 6988
- (1994) Tetrahedron , vol.50 , pp. 6975-6988
- Shabana, R.¹ Osman, F.H.² Atrees, S.S.³

20
- 49149122173
- J.A. Seijas, M.P. Vázquez-Tato, and J. Crecente-Campo Tetrahedron 64 2008 9280 9285
- (2008) Tetrahedron , vol.64 , pp. 9280-9285
- Seijas, J.A.¹ Vázquez-Tato, M.P.² Crecente-Campo, J.³

21
- 0035813242
- L. Perreux, and A. Loupy Tetrahedron 57 2001 9199 9223
- (2001) Tetrahedron , vol.57 , pp. 9199-9223
- Perreux, L.¹ Loupy, A.²

22
- 84963255831
- R. Shabana, and S.S. Atrees Phosphorus, Sulfur, Silicon Relat. Elem. 105 1995 57 62
- (1995) Phosphorus, Sulfur, Silicon Relat. Elem. , vol.105 , pp. 57-62
- Shabana, R.¹ Atrees, S.S.²

23
- 0011655731
- N.M. Yousif, R. Shabana, and S.O. Lawesson Bull. Soc. Chim. Fr. 1986 283 287
- (1986) Bull. Soc. Chim. Fr. , pp. 283-287
- Yousif, N.M.¹ Shabana, R.² Lawesson, S.O.³

24
- 27744478527
- X.Q. Shen, H.L. Liu, H.Y. Zhang, H.Q. Zhang, H.Y. Mao, Q.A. Wu, Y. Zhu, and H.W. Hou Chinese J. Struct. Chem. 24 2005 1211 1216
- (2005) Chinese J. Struct. Chem. , vol.24 , pp. 1211-1216
- Shen, X.Q.¹ Liu, H.L.² Zhang, H.Y.³ Zhang, H.Q.⁴ Mao, H.Y.⁵ Wu, Q.A.⁶ Zhu, Y.⁷ Hou, H.W.⁸

25
- 77956618601
- For dioxaphospholes (9a-c) the reaction time was 5 min
- For dioxaphospholes (9a-c) the reaction time was 5 min.

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.