SCOPUS 정보 검색 플랫폼

Volumn , Issue 41, 2009, Pages 6210-6212

NeoPHOX - An easily accessible P,N-ligand for iridium-catalyzed asymmetric hydrogenation: Preparation, scope and application in the synthesis of demethyl methoxycalamenene

(2) Schrems, Marcus G a Pfaltz, Andreas a

a UNIVERSITY OF BASEL (Switzerland)

Author keywords

[No Author keywords available]

Indexed keywords

CHLORO ALKYLOXAZOLINE DERIVATIVE; DEMETHYL METHOXYCALAMENENE; IRIDIUM; LIGAND; OXAZOLINE DERIVATIVE; PHOSPHINO OXAZOLINE DERIVATIVE; TERPENE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CATALYSIS; CHEMICAL STRUCTURE; HYDROGENATION;

EID: 70349915666 PISSN: 13597345 EISSN: None Source Type: Journal
DOI: 10.1039/b912680e Document Type: Article

Times cited : (65)

References (18)

1
- 0032476793
- A. Lightfoot P. Schnider A. Pfaltz Angew. Chem., Int. Ed. 1998 37 2897
- (1998) Angew. Chem., Int. Ed. , vol.37 , pp. 2897
- Lightfoot, A.¹ Schnider, P.² Pfaltz, A.³

2
- 38049078593
- S. J. Roseblade A. Pfaltz Acc. Chem. Res. 2007 40 1402
- (2007) Acc. Chem. Res. , vol.40 , pp. 1402
- Roseblade, S.J.¹ Pfaltz, A.²

3
- 33646048747
- K. Källström I. Munslow P. G. Andersson Chem.-Eur. J. 2006 12 3194
- (2006) Chem.-Eur. J. , vol.12 , pp. 3194
- Källström, K.¹ Munslow, I.² Andersson, P.G.³

4
- 26444468950
- Currently, the only commercially available chiral iridium hydrogenation catalysts are two ThrePHOX-complexes:
- X. Cui K. Burgess Chem. Rev. 2005 105 3272
- (2005) Chem. Rev. , vol.105 , pp. 3272
- Cui, X.¹ Burgess, K.²

5
- 0002636574
- F. Menges A. Pfaltz Adv. Synth. Catal. 2002 344 40
- (2002) Adv. Synth. Catal. , vol.344 , pp. 40
- Menges, F.¹ Pfaltz, A.²

6
- 3042715450
- S. P. Smidt F. Menges A. Pfaltz Org. Lett. 2004 6 2023
- (2004) Org. Lett. , vol.6 , pp. 2023
- Smidt, S.P.¹ Menges, F.² Pfaltz, A.³

7
- 36049040593
- M. G. Schrems E. Neumann A. Pfaltz Angew. Chem., Int. Ed. 2007 46 8274
- (2007) Angew. Chem., Int. Ed. , vol.46 , pp. 8274
- Schrems, M.G.¹ Neumann, E.² Pfaltz, A.³

8
- 64149115224
- M. G. Schrems E. Neumann A. Pfaltz Heterocycles 2008 76 771
- (2008) Heterocycles , vol.76 , pp. 771
- Schrems, M.G.¹ Neumann, E.² Pfaltz, A.³

9
- 0037239899
- R. A. Rossi A. B. Pierini A. B. Peñéñory Chem. Rev. 2003 103 71
- (2003) Chem. Rev. , vol.103 , pp. 71
- Rossi, R.A.¹ Pierini, A.B.² Peñéñory, A.B.³

10
- 0000331564
- G. M. Atkins E. M. Burgess J. Am. Chem. Soc. 1968 90 4744
- (1968) J. Am. Chem. Soc. , vol.90 , pp. 4744
- Atkins, G.M.¹ Burgess, E.M.²

11
- 0006089507
- F. Bohlmann C. Zdero H. Robinson R. King Phytochemistry 1979 18 1675
- (1979) Phytochemistry , vol.18 , pp. 1675
- Bohlmann, F.¹ Zdero, C.² Robinson, H.³ King, R.⁴

12
- 33748969164
- L. F. Tietze T. Raschke Liebigs Ann. 1996 1981
- (1996) Liebigs Ann. , pp. 1981
- Tietze, L.F.¹ Raschke, T.²

13
- 0006043219
- L. F. Tietze T. Raschke Synlett 1995 597
- (1995) Synlett , pp. 597
- Tietze, L.F.¹ Raschke, T.²

14
- 67749114483
- K. C. Nicolaou R. Reingruber D. Sarlah S. Bräse J. Am. Chem. Soc. 2009 131 2086
- (2009) J. Am. Chem. Soc. , vol.131 , pp. 2086
- Nicolaou, K.C.¹ Reingruber, R.² Sarlah, D.³ Bräse, S.⁴

15
- 70149099966
- erratum J. Am. Chem. Soc. 2009 131 6640
- erratum J. Am. Chem. Soc. 2009 131 6640

16
- 0141854100
- H. G. Schmalz O. Kiehl U. Korell J. Lex Synthesis 2003 1851
- (2003) Synthesis , pp. 1851
- Schmalz, H.G.¹ Kiehl, O.² Korell, U.³ Lex, J.⁴

17
- 33746929105
- M. Hatano S. Suzuki K. Ishihara J. Am. Chem. Soc. 2006 128 9998
- (2006) J. Am. Chem. Soc. , vol.128 , pp. 9998
- Hatano, M.¹ Suzuki, S.² Ishihara, K.³

18
- 84977699543
- Without the recrystallization of 15 the overall yield would be 37% (46% based on recovered starting material), with an enantiomeric excess of 93%
- H. Vollmann H. Becker M. Corell H. Streeck G. Langbein Justus Liebigs Ann. Chem. 1937 531 1
- (1937) Justus Liebigs Ann. Chem. , vol.531 , pp. 1
- Vollmann, H.¹ Becker, H.² Corell, M.³ Streeck, H.⁴ Langbein, G.⁵

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.