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Journal of Organic Chemistry

Volumn 76, Issue 10, 2011, Pages 4168-4172

Resolution of carboxylic acids using copper(I)-promoted removal of propargylic esters under neutral conditions

(2) Ghosh, Partha a Aubé, Jeffrey a

a UNIVERSITY OF KANSAS (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CHROMATOGRAPHIC SEPARATIONS; DIASTEREOMERIC; DIASTEREOMERS; ENANTIOMERIC RATIO; ESTER HYDROLYSIS; GOOD YIELD; NEUTRAL CONDITIONS; OPTICAL RESOLUTION; PROPARGYL ALCOHOL; PROPARGYLIC ESTER;

COPYING; ESTERIFICATION; ESTERS; LIQUID CHROMATOGRAPHY; METHANOL;

CARBOXYLIC ACIDS;

ALCOHOL DERIVATIVE; CARBOXYLIC ACID; COPPER ION; ESTER; FUNCTIONAL GROUP; PROPARGYLIC ESTER DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CATALYSIS; CHROMATOGRAPHY; CRYSTALLIZATION; ENANTIOMER; EPIMERIZATION; HYDROLYSIS; POLYMERIZATION; REACTION TIME; STEREOCHEMISTRY; SUBSTITUTION REACTION;

ALKYNES; CARBOXYLIC ACIDS; CHROMATOGRAPHY; COPPER; ESTERS; HYDROGEN-ION CONCENTRATION; STEREOISOMERISM;

EID: 79956108920 PISSN: 00223263 EISSN: 15206904 Source Type: Journal
DOI: 10.1021/jo200433w Document Type: Article

Times cited : (8)

References (16)

1
- 0004139080
- Reviews:; Wiley-Interscience: New York
- Reviews: Jacques, J.; Collet, A.; Wilen, S. H. Enantiomers, Racemates and Resolutions; Wiley-Interscience: New York, 1981.
- (1981) Enantiomers, Racemates and Resolutions
- Jacques, J.¹ Collet, A.² Wilen, S.H.³

2
- 70349674542
- Porter, W. H. Pure Appl. Chem. 1991, 63, 1119-1122
- (1991) Pure Appl. Chem. , vol.63 , pp. 1119-1122
- Porter, W.H.¹

3
- 77954708872
- Sekhon, B. S. Int. J. PharmTech Res. 2010, 2, 1584-1594
- (2010) Int. J. PharmTech Res. , vol.2 , pp. 1584-1594
- Sekhon, B.S.¹

4
- 36649037808
- Frankowski, K. J.; Hirt, E. E.; Zeng, Y.; Neuenswander, B.; Fowler, D.; Schoenen, F.; Aubé, J. J. Comb. Chem. 2007, 9, 1188-1192
- (2007) J. Comb. Chem. , vol.9 , pp. 1188-1192
- Frankowski, K.J.¹ Hirt, E.E.² Zeng, Y.³ Neuenswander, B.⁴ Fowler, D.⁵ Schoenen, F.⁶ Aubé, J.⁷

5
- 77956162799
- Frankowski, K. J.; Ghosh, P.; Setola, V.; Tran, T. B.; Roth, B. L.; Aubé, J. ACS Med. Chem. Lett. 2010, 1, 189-193
- (2010) ACS Med. Chem. Lett. , vol.1 , pp. 189-193
- Frankowski, K.J.¹ Ghosh, P.² Setola, V.³ Tran, T.B.⁴ Roth, B.L.⁵ Aubé, J.⁶

6
- 0028238209
- Yamada, Y.; Yuasa, M.; Nakamura, I.; Murahashi, S. J. Org. Chem. 1994, 59, 2282-2284
- (1994) J. Org. Chem. , vol.59 , pp. 2282-2284
- Yamada, Y.¹ Yuasa, M.² Nakamura, I.³ Murahashi, S.⁴

7
- 45549088523
- Detz, R. J.; Delville, M. M. E.; Hiemstra, H.; van Maarseveen, J. H. Angew. Chem., Int. Ed. 2008, 47, 3777-3780
- (2008) Angew. Chem., Int. Ed. , vol.47 , pp. 3777-3780
- Detz, R.J.¹ Delville, M.M.E.² Hiemstra, H.³ Van Maarseveen, J.H.⁴

8
- 0034665126
- Mahrwald, R.; Quint, S. Tetrahedron 2000, 56, 7463-7468
- (2000) Tetrahedron , vol.56 , pp. 7463-7468
- Mahrwald, R.¹ Quint, S.²

9
- 84874446846
- For a review of the Glaser coupling of alkynes, see: In Part 1;, Part 1 Ed.; John Wiley & Sons, Inc.: Hoboken, NJ,; pp - 257
- For a review of the Glaser coupling of alkynes, see: Gribble, G. W. In NameReactions for Homologation, Part 1; Li, J. J., Part 1 Ed.; John Wiley & Sons, Inc.: Hoboken, NJ, 2009; pp 236 - 257.
- (2009) NameReactions for Homologation , pp. 236
- Gribble, G.W.¹ Li, J.J.²

10
- 79956073784
- Carboxylic acids 5 - 8 are commercially available and 9 is known (ref 2b)
- Carboxylic acids 5 - 8 are commercially available and 9 is known (ref 2b).

11
- 0030000285
- Waldinger, C.; Schneider, M.; Botta, M.; Corelli, F.; Summa, V. Tetrahedron: Asymmetry 1996, 7, 1485-1488
- (1996) Tetrahedron: Asymmetry , vol.7 , pp. 1485-1488
- Waldinger, C.¹ Schneider, M.² Botta, M.³ Corelli, F.⁴ Summa, V.⁵

12
- 0027427886
- Baldoli, C.; Buttero, P. D.; Licandro, E.; Maiorana, S.; Papagni, A.; Torchio, M. Tetrahedron Lett. 1993, 34, 7943-7946
- (1993) Tetrahedron Lett. , vol.34 , pp. 7943-7946
- Baldoli, C.¹ Buttero, P.D.² Licandro, E.³ Maiorana, S.⁴ Papagni, A.⁵ Torchio, M.⁶

13
- 79956089350
- Authentic samples were prepared by reacting racemic 1-(2-methoxyphenyl) prop-2-yn-1-ol with l -Boc-proline, diastereomer separation, and hydrolysis with LiOH
- Authentic samples were prepared by reacting racemic 1-(2-methoxyphenyl) prop-2-yn-1-ol with l -Boc-proline, diastereomer separation, and hydrolysis with LiOH.

14
- 79956104966
- Carboxylic acid (4a S,8 S,8a R)- 9 was converted to the analogous 4-bromo-2-(trifluoromethyl)aniline amide, which was subjected to anomalous X-ray diffraction to determine the absolute stereochemistry
- Carboxylic acid (4a S,8 S,8a R)- 9 was converted to the analogous 4-bromo-2-(trifluoromethyl)aniline amide, which was subjected to anomalous X-ray diffraction to determine the absolute stereochemistry.

15
- 74849085536
- Kumar, P. S.; Banerjee, A.; Baskaran, S. Angew. Chem., Int. Ed. 2010, 49, 804-807
- (2010) Angew. Chem., Int. Ed. , vol.49 , pp. 804-807
- Kumar, P.S.¹ Banerjee, A.² Baskaran, S.³

16
- 37049124660
- Hagishita, S.; Kuriyama, K. J. Chem. Soc., Perkin. Trans. 2 1974, 6, 686-696
- (1974) J. Chem. Soc., Perkin. Trans. 2 , vol.6 , pp. 686-696
- Hagishita, S.¹ Kuriyama, K.²

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