SCOPUS 정보 검색 플랫폼

Volumn 54, Issue 17, 2015, Pages 5009-5011

Thrilling strain! Donor-acceptor-substituted cyclobutanes for the synthesis of (hetero)cyclic compounds

Author keywords

cycloaddition; cyclobutanes; homogeneous catalysis; photochemistry; pyrans

Indexed keywords

CYCLOADDITION; PHOTOCHEMICAL REACTIONS; STEREOCHEMISTRY; STEREOSELECTIVITY;

CYCLIC COMPOUNDS; CYCLOBUTANES; DONOR ACCEPTORS; HETEROCYCLES; HOMOGENEOUS CATALYSIS; PYRANS; RING STRAINS; STEREOSELECTIVE SYNTHESIS;

REACTION KINETICS;

EID: 84927739573 PISSN: 14337851 EISSN: 15213773 Source Type: Journal
DOI: 10.1002/anie.201501135 Document Type: Article

Times cited : (55)

References (29)

1
- 0000662936
- A. de Meijere, Angew. Chem. Int. Ed. Engl. 1979, 18, 809-826
- (1979) Angew. Chem. Int. Ed. Engl. , vol.18 , pp. 809-826
- De Meijere, A.¹

2
- 0000645462
- Angew. Chem. 1979, 91, 867-884
- (1979) Angew. Chem. , vol.91 , pp. 867-884

3
- 80051754886
- review on cyclobutanes in catalysis
- review on cyclobutanes in catalysis:, T. Seiser, T. Saget, D. N. Tran, N. Cramer, Angew. Chem. Int. Ed. 2011, 50, 7740-7752
- (2011) Angew. Chem. Int. Ed. , vol.50 , pp. 7740-7752
- Seiser, T.¹ Saget, T.² Tran, D.N.³ Cramer, N.⁴

4
- 84859942190
- Angew. Chem. 2011, 123, 7884-7896.
- (2011) Angew. Chem. , vol.123 , pp. 7884-7896

5
- 84985628264
- The term donor-acceptor-substituted cyclopropane was introduced in 1980
- The term donor-acceptor-substituted cyclopropane was introduced in 1980:, H.-U. Reissig, E. Hirsch, Angew. Chem. Int. Ed. Engl. 1980, 19, 813-814
- (1980) Angew. Chem. Int. Ed. Engl. , vol.19 , pp. 813-814
- Reissig, H.-U.¹ Hirsch, E.²

6
- 4243507204
- review
- Angew. Chem. 1980, 92, 839-840; review
- (1980) Angew. Chem. , vol.92 , pp. 839-840

7
- 0001796781
- From consideration of Wenkert's seminal investigations on oxycyclopropanes (see Ref. [3a]), D-A cyclopropanes were defined as compounds with "strong" donor substituents such as RO or R2N groups; the term is nowadays also applied to compounds with other donor groups (e.g. aryl)
- H.-U. Reissig, Top. Curr. Chem. 1988, 144, 73-135. From consideration of Wenkert's seminal investigations on oxycyclopropanes (see Ref. [3a]), D-A cyclopropanes were defined as compounds with "strong" donor substituents such as RO or R2N groups; the term is nowadays also applied to compounds with other donor groups (e.g. aryl).
- (1988) Top. Curr. Chem. , vol.144 , pp. 73-135
- Reissig, H.-U.¹

8
- 0002631111
- E. Wenkert, Acc. Chem. Res. 1980, 13, 27-31
- (1980) Acc. Chem. Res. , vol.13 , pp. 27-31
- Wenkert, E.¹

9
- 0037884930
- H.-U. Reissig, R. Zimmer, Chem. Rev. 2003, 103, 1151-1196
- (2003) Chem. Rev. , vol.103 , pp. 1151-1196
- Reissig, H.-U.¹ Zimmer, R.²

10
- 9744249469
- M. Yu, B. L. Pagenkopf, Tetrahedron 2005, 61, 321-347
- (2005) Tetrahedron , vol.61 , pp. 321-347
- Yu, M.¹ Pagenkopf, B.L.²

11
- 70350512114
- C. A. Carson, M. A. Kerr, Chem. Soc. Rev. 2009, 38, 3051-3060
- (2009) Chem. Soc. Rev. , vol.38 , pp. 3051-3060
- Carson, C.A.¹ Kerr, M.A.²

12
- 84892410356
- M. A. Cavitt, L. H. Phun, S. France, Chem. Soc. Rev. 2014, 43, 804-818
- (2014) Chem. Soc. Rev. , vol.43 , pp. 804-818
- Cavitt, M.A.¹ Phun, L.H.² France, S.³

13
- 84901449253
- T. F. Schneider, J. Kaschel, D. Werz, Angew. Chem. Int. Ed. 2014, 53, 5504-5523
- (2014) Angew. Chem. Int. Ed. , vol.53 , pp. 5504-5523
- Schneider, T.F.¹ Kaschel, J.² Werz, D.³

14
- 84919385987
- Angew. Chem. 2014, 126, 5608-5628.
- (2014) Angew. Chem. , vol.126 , pp. 5608-5628

15
- 84855959119
- R. Okado, A. Nowaki, J.-i. Matsuo, H. Ishibashi, Chem. Pharm. Bull. 2012, 60, 21-22
- (2012) Chem. Pharm. Bull. , vol.60 , pp. 21-22
- Okado, R.¹ Nowaki, A.² Matsuo, J.-I.³ Ishibashi, H.⁴

16
- 84898047585
- short review
- short review:, J.-i. Matsuo, Tetrahedron Lett. 2014, 55, 2589-2595
- (2014) Tetrahedron Lett. , vol.55 , pp. 2589-2595
- Matsuo, J.-I.¹

17
- 0011562591
- see also
- see also:, S. Shimada, K. Saigo, H. Nakamura, M. Hasegawa, Chem. Lett. 1991, 1149-1152.
- (1991) Chem. Lett. , pp. 1149-1152
- Shimada, S.¹ Saigo, K.² Nakamura, H.³ Hasegawa, M.⁴

18
- 84892862060
- N. Vemula, A. C. Stevens, T. B. Schon, B. L. Pagenkopf, Chem. Commun. 2014, 50, 1668-1670.
- (2014) Chem. Commun. , vol.50 , pp. 1668-1670
- Vemula, N.¹ Stevens, A.C.² Schon, T.B.³ Pagenkopf, B.L.⁴

19
- 79952594276
- A. C. Stevens, C. Palmer, B. L. Pagenkopf, Org. Lett. 2011, 13, 1528-1531.
- (2011) Org. Lett. , vol.13 , pp. 1528-1531
- Stevens, A.C.¹ Palmer, C.² Pagenkopf, B.L.³

20
- 84906568615
- Review
- Review:, F. de Nanteuil, F. De Simone, R. Frei, F. Benfatt, E. Serrano, J. Waser, Chem. Commun. 2014, 50, 10912-10928.
- (2014) Chem. Commun. , vol.50 , pp. 10912-10928
- De Nanteuil, F.¹ De Simone, F.² Frei, R.³ Benfatt, F.⁴ Serrano, E.⁵ Waser, J.⁶

21
- 84882266189
- F. de Nanteuil, J. Waser, Angew. Chem. Int. Ed. 2013, 52, 9009-9013
- (2013) Angew. Chem. Int. Ed. , vol.52 , pp. 9009-9013
- De Nanteuil, F.¹ Waser, J.²

22
- 84899809512
- Angew. Chem. 2013, 125, 9179-9183.
- (2013) Angew. Chem. , vol.125 , pp. 9179-9183

23
- 84923382868
- D. Perrotta, S. Racine, J. Vuilleumier, F. de Nanteuil, J. Waser, Org. Lett. 2015, 17, 1030-1033.
- (2015) Org. Lett. , vol.17 , pp. 1030-1033
- Perrotta, D.¹ Racine, S.² Vuilleumier, J.³ De Nanteuil, F.⁴ Waser, J.⁵

24
- 84919341257
- R. Shenje, M. C. Martin, S. France, Angew. Chem. Int. Ed. 2014, 53, 13907-13911
- (2014) Angew. Chem. Int. Ed. , vol.53 , pp. 13907-13911
- Shenje, R.¹ Martin, M.C.² France, S.³

25
- 84927774164
- Angew. Chem. 2014, 126, 14127-14131.
- (2014) Angew. Chem. , vol.126 , pp. 14127-14131

26
- 33947292540
- Review
- Review:, P. de Mayo, Acc. Chem. Res. 1971, 4, 41-47.
- (1971) Acc. Chem. Res. , vol.4 , pp. 41-47
- De Mayo, P.¹

27
- 84941112288
- R. Brimioulle, T. Bach, Angew. Chem. Int. Ed. 2014, 53, 12921-12924
- (2014) Angew. Chem. Int. Ed. , vol.53 , pp. 12921-12924
- Brimioulle, R.¹ Bach, T.²

28
- 84924866246
- Angew. Chem. 2014, 126, 13135-13138.
- (2014) Angew. Chem. , vol.126 , pp. 13135-13138

29
- 84907718657
- For strained D-A cyclopentanes, see, M. M. Walker, C. G. Goodman, J. S. Johnson, J. Org. Chem. 2014, 79, 9385-9388.
- (2014) J. Org. Chem. , vol.79 , pp. 9385-9388
- Walker, M.M.¹ Goodman, C.G.² Johnson, J.S.³

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.