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Chemical Communications

Volumn , Issue 16, 2000, Pages 1521-1522

Diastereoselective epoxide rearrangements using lithium amide bases: First stereocontrolled synthesis of 4-deoxyconduritols

(4) Kee, A a O'Brien, P a Pilgram, C D a Watson, S T a

a UNIVERSITY OF YORK (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ALCOHOL DERIVATIVE;

ARTICLE; CHEMICAL REACTION; REACTION ANALYSIS; STEREOCHEMISTRY; SYNTHESIS;

EID: 0034699166 PISSN: 13597345 EISSN: None Source Type: Journal
DOI: 10.1039/b003717f Document Type: Article

Times cited : (24)

References (17)

1
- 0008486562
- Cyclitols and Derivatives. V.C.H. New York
- (1993)
- Hudlicky, T.¹ Cebulak, M.²

2
- 0033533796
- (1999) J. Chem. Soc., Chem. Commun. , pp. 1985
- Honzumi, M.¹ Hiroya, K.² Taniguchi, T.³ Ogasawara, K.⁴

3
- 0003060550
- (1998) J. Chem. Soc., Chem. Commun. , pp. 1945
- Kim, K.S.¹ Park, J.I.² Moon, H.K.³ Yi, H.⁴

4
- 0030962375
- (1997) J. Org. Chem. , vol.62 , pp. 2453
- Salamci, E.¹ Secen, H.² Sutbeyaz, Y.³ Balci, M.⁴

5
- 0032508069
- (1998) Tetrahedron Lett. , vol.39 , pp. 4393
- Haines, A.H.¹ King, A.S.H.² Knight, J.R.³ Nguyen, V.-A.⁴

6
- 0000453450
- (1998) J. Org. Chem. , vol.63 , pp. 2039
- Maras, A.¹ Secen, H.² Sutbeyaz, Y.³ Balci, M.⁴

7
- 0033531992
- (1999) Tetrahedron Lett. , vol.40 , pp. 3781
- Maezaki, N.¹ Nagahashi, N.² Yoshigami, R.³ Iwata, C.⁴ Tanaka, T.⁵

8
- 26644457235
- (1998) J. Chem. Soc., Perkin Trans. , vol.1 , pp. 2435
- O'Brien, P.¹ Poumellec, P.²

9
- 0033607743
- (1999) Tetrahedron Lett. , vol.40 , pp. 8423
- De Sousa, S.E.¹ O'Brien, P.² Steffens, H.C.³

10
- 0001612545
- (1969) J. Org. Chem. , vol.34 , pp. 3583
- Rickborn, B.¹ Thummel, R.P.²

11
- 0001117008
- (1983) Org. React. (N.Y.) , vol.29 , pp. 345
- Crandall, J.K.¹ Apparu, M.²

12
- 33748957377
- (1997) J. Chem. Soc. Perkin Trans. , vol.1 , pp. 2023
- Hense, A.¹ Ley, S.V.² Osborn, H.M.I.³ Owen, D.R.⁴ Poisson, J.-F.⁵ Warriner, S.L.⁶ Wesson, K.E.⁷

13
- 1542396822
- (1996) Synlett , pp. 793
- Douglas, N.L.¹ Ley, S.V.² Osborn, H.M.I.³ Owen, D.R.⁴ Priepke, H.W.M.⁵ Warriner, S.L.⁶

14
- 0000948848
- (1996) J. Org. Chem. , vol.61 , pp. 3897
- Montchamp, J.-L.¹ Tian, F.² Hart, M.E.³ Frost, J.W.⁴

15
- 0001627220
- (1987) Tetrahedron , vol.43 , pp. 2249
- Mori, K.¹ Hazra, B.G.² Pfeiffer, R.J.³ Gupta, A.K.⁴ Lindgren, B.S.⁵

16
- 0000196539
- (1989) Tetrahedron Lett. , vol.30 , pp. 2125
- Asami, M.¹ Kanemaki, N.²

17
- 0008449371
- Since we usually use 2 equiv. of chiral lithium amide bases for epoxide rearrangement reactions, we decided to use 0.7 equiv. of chiral base for the kinetic resolution. When 0.5 equiv. of chiral base was used, we obtained a 26% yield of allylic alcohol 11 (64% ee)

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