SCOPUS 정보 검색 플랫폼

Volumn 15, Issue 6, 2013, Pages 1608-1614

Engaging isatins in solvent-free, sterically congested Passerini reaction

Author keywords

[No Author keywords available]

Indexed keywords

EID: 84884186258 PISSN: 14639262 EISSN: 14639270 Source Type: Journal
DOI: 10.1039/c3gc40454d Document Type: Article

Times cited : (22)

References (31)

1
- 0001685385
- M. Passerini Gazz. Chim. Ital. 1921 51 126
- (1921) Gazz. Chim. Ital. , vol.51 , pp. 126
- Passerini, M.¹

2
- 0040537649
- for a review, see
- M. Passerini Gazz. Chim. Ital. 1922 52 432
- (1922) Gazz. Chim. Ital. , vol.52 , pp. 432
- Passerini, M.¹

3
- 11444268106
- in, ed. A. B. Charette, Wiley, New York, 1-140 For a review, see
- L. Banfi and R. Riva, in Organic Reactions, ed., A. B. Charette, Wiley, New York, 2005, vol. 65, pp. 1-140
- (2005) Organic Reactions , vol.65
- Banfi, L.¹ Riva, R.²

4
- 2542509173
- For reviews, see
- A. Dömling I. Ugi Angew. Chem., Int. Ed. 2000 39 3168
- (2000) Angew. Chem., Int. Ed. , vol.39 , pp. 3168
- Dömling, A.¹ Ugi, I.²

5
- 31544434530
- A. Dömling Chem. Rev. 2006 106 17
- (2006) Chem. Rev. , vol.106 , pp. 17
- Dömling, A.¹

6
- 84862175237
- A. Dömling W. Wang K. Wang Chem. Rev. 2012 112 3083
- (2012) Chem. Rev. , vol.112 , pp. 3083
- Dömling, A.¹ Wang, W.² Wang, K.³

7
- 84890597202
- ed., Wiley-VCH, Weinheim,; for a recent report on the synthesis of 4-fluoro glutamines, see
- Multicomponent Reactions, ed., J. Zhu, and, H. Bienaymé, Wiley-VCH, Weinheim, 2005; for a recent report on the synthesis of 4-fluoro glutamines, see
- (2005) Multicomponent Reactions
- Zhu, J.¹ Bienaymé, H.²

8
- 79851483342
- For a review on heterocyclic construction using isocyanides, see
- W. Qu Z. Zha K. Ploessl B. P. Lieberman L. Zhu D. R. Wise C. B. Thompson H. F. Kung J. Am. Chem. Soc. 2011 133 1122
- (2011) J. Am. Chem. Soc. , vol.133 , pp. 1122
- Qu, W.¹ Zha, Z.² Ploessl, K.³ Lieberman, B.P.⁴ Zhu, L.⁵ Wise, D.R.⁶ Thompson, C.B.⁷ Kung, H.F.⁸

9
- 0348147693
- V. Nair C. Rajesh A. U. Vinod S. Bindu A. R. Sreekanth J. S. Mathen L. Balagopal Acc. Chem. Res. 2003 36 899
- (2003) Acc. Chem. Res. , vol.36 , pp. 899
- Nair, V.¹ Rajesh, C.² Vinod, A.U.³ Bindu, S.⁴ Sreekanth, A.R.⁵ Mathen, J.S.⁶ Balagopal, L.⁷

10
- 0003172436
- M. Passerini Gazz. Chim. Ital. 1924 54 529
- (1924) Gazz. Chim. Ital. , vol.54 , pp. 529
- Passerini, M.¹

11
- 0009956053
- for a recent report on the Passerini three-component reaction of alcohols under catalytic and aerobic oxidative conditions, see
- R. Baker A. H. Schlesinger J. Am. Chem. Soc. 1945 67 1499
- (1945) J. Am. Chem. Soc. , vol.67 , pp. 1499
- Baker, R.¹ Schlesinger, A.H.²

12
- 77950292795
- J. Brioche G. Masson J. Zhu Org. Lett. 2010 12 1432
- (2010) Org. Lett. , vol.12 , pp. 1432
- Brioche, J.¹ Masson, G.² Zhu, J.³

13
- 84867846140
- C. Cui C. Zhu X.-J. Du Z.-P. Wang Z.-M. Li W.-G. Zhao Green Chem. 2012 14 3157
- (2012) Green Chem. , vol.14 , pp. 3157
- Cui, C.¹ Zhu, C.² Du, X.-J.³ Wang, Z.-P.⁴ Li, Z.-M.⁵ Zhao, W.-G.⁶

14
- 0037060017
- For recent reviews, see
- G. Jenner Tetrahedron Lett. 2002 43 1235
- (2002) Tetrahedron Lett. , vol.43 , pp. 1235
- Jenner, G.¹

15
- 84869188848
- G. S. Singh Z. Y. Desta Chem. Rev. 2012 112 6104
- (2012) Chem. Rev. , vol.112 , pp. 6104
- Singh, G.S.¹ Desta, Z.Y.²

16
- 84867324818
- For selected reports, see
- R. Dalpozzo G. Bartolib G. Bencivennib Chem. Soc. Rev. 2012 41 7247
- (2012) Chem. Soc. Rev. , vol.41 , pp. 7247
- Dalpozzo, R.¹ Bartolib, G.² Bencivennib, G.³

17
- 33751290436
- G. Luppi M. Monari R. J. Corrêa F. A. Violante A. C. Pinto B. Kaptein Q. B. Broxterman S. J. Garden C. Tomasini Tetrahedron 2006 62 12017
- (2006) Tetrahedron , vol.62 , pp. 12017
- Luppi, G.¹ Monari, M.² Corrêa, R.J.³ Violante, F.A.⁴ Pinto, A.C.⁵ Kaptein, B.⁶ Broxterman, Q.B.⁷ Garden, S.J.⁸ Tomasini, C.⁹

18
- 33644772040
- For selected examples, see
- T. Nakamura S.-I. Shirokawa S. Hosokawa A. Nakazaki S. Kobayashi Org. Lett. 2006 8 677
- (2006) Org. Lett. , vol.8 , pp. 677
- Nakamura, T.¹ Shirokawa, S.-I.² Hosokawa, S.³ Nakazaki, A.⁴ Kobayashi, S.⁵

19
- 79251553475
- Z. Zhang W. Zheng J. C. Antilla Angew. Chem., Int. Ed. 2011 50 1135
- (2011) Angew. Chem., Int. Ed. , vol.50 , pp. 1135
- Zhang, Z.¹ Zheng, W.² Antilla, J.C.³

20
- 79955371062
- A. Singh G. P. Roth Org. Lett. 2011 13 2118
- (2011) Org. Lett. , vol.13 , pp. 2118
- Singh, A.¹ Roth, G.P.²

21
- 0035924185
- For recent reports on solvent-free Passerini reactions using aldehydes as the carbonyl component, see
- T. Tokunaga W. E. Hume T. Umezome K. Okazaki Y. Ueki K. Kumagai S. Hourai J. Nagamine H. Seki M. Taiji H. Noguchi R. Nagata J. Med. Chem. 2001 44 4641
- (2001) J. Med. Chem. , vol.44 , pp. 4641
- Tokunaga, T.¹ Hume, W.E.² Umezome, T.³ Okazaki, K.⁴ Ueki, Y.⁵ Kumagai, K.⁶ Hourai, S.⁷ Nagamine, J.⁸ Seki, H.⁹ Taiji, M.¹⁰ Noguchi, H.¹¹ Nagata, R.¹²

22
- 84872184089
- K. Sato T. Ozu N. Takenaga Tetrahedron Lett. 2013 54 661
- (2013) Tetrahedron Lett. , vol.54 , pp. 661
- Sato, K.¹ Ozu, T.² Takenaga, N.³

23
- 83555166320
- T. Bousquet M. Jida M. Soueidan R. Deprez-Poulain F. Agbossou-Niedercorn L. Pelinski Tetrahedron Lett. 2012 53 306
- (2012) Tetrahedron Lett. , vol.53 , pp. 306
- Bousquet, T.¹ Jida, M.² Soueidan, M.³ Deprez-Poulain, R.⁴ Agbossou-Niedercorn, F.⁵ Pelinski, L.⁶

24
- 40549113025
- 3CN proceeding in the presence of 4 Å molecular sieves was reported by Esmaeili et al. For details, see
- D. Koszelewski W. Szymanski J. Krysiak R. Ostaszewski Synth. Commun. 2008 28 1120
- (2008) Synth. Commun. , vol.28 , pp. 1120
- Koszelewski, D.¹ Szymanski, W.² Krysiak, J.³ Ostaszewski, R.⁴

25
- 84871298326
- Notably, this protocol is not applicable under solvent-free conditions and with bulky isocyanides including tert-butyl isocyanide and proceeds only in the presence of additives It may be noted that pyrrole 2-carboxylic acid afforded the desired product in ∼15% yield In addition, α-amino acids such as (l) phenyl alanine as well as (l) proline did not show any reactivity under the present reaction conditions. For a successful application of α-amino acids in a multicomponent reaction, see
- A. A. Esmaeili S. A. Ghalandarabad S. Jannati Tetrahedron Lett. 2013 54 406
- (2013) Tetrahedron Lett. , vol.54 , pp. 406
- Esmaeili, A.A.¹ Ghalandarabad, S.A.² Jannati, S.³

26
- 0347915136
- For related reports, see
- A. Demharter W. Hörl E. Herdtweck I. Ugi Angew. Chem., Int. Ed. Engl. 1996 35 173
- (1996) Angew. Chem., Int. Ed. Engl. , vol.35 , pp. 173
- Demharter, A.¹ Hörl, W.² Herdtweck, E.³ Ugi, I.⁴

27
- 29144448797
- L. El Kaïm L. Grimaud J. Oble Angew. Chem., Int. Ed. 2005 44 7961
- (2005) Angew. Chem., Int. Ed. , vol.44 , pp. 7961
- El Kaïm, L.¹ Grimaud, L.² Oble, J.³

28
- 33750929343
- For recent reviews on one-pot reactions, see
- L. El Kaim M. Gizolme L. Grimaud Org. Lett. 2006 8 5021
- (2006) Org. Lett. , vol.8 , pp. 5021
- El Kaim, L.¹ Gizolme, M.² Grimaud, L.³

29
- 80052442679
- Ł. Albrecht H. Jiang K. A. Jørgensen Angew. Chem., Int. Ed. 2011 50 8492
- (2011) Angew. Chem., Int. Ed. , vol.50 , pp. 8492
- Albrecht, Ł.¹ Jiang, H.² Jørgensen, K.A.³

30
- 79951685909
- M. J. Climent A. Corma S. Iborra Chem. Rev. 2011 111 1072
- (2011) Chem. Rev. , vol.111 , pp. 1072
- Climent, M.J.¹ Corma, A.² Iborra, S.³

31
- 34347335758
- A. M. Walji D. W. C. MacMillan Synlett 2007 1477
- (2007) Synlett , pp. 1477
- Walji, A.M.¹ Macmillan, D.W.C.²

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.