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Tetrahedron Letters

Volumn 28, Issue 10, 1987, Pages 1069-1072

Pyridinium dichromate-induced 1,3-oxidative rearrangements of enynols

(4) Liotta, Dennis a Brown, David a Hoekstra, William a Monahan III, Robert a

a EMORY UNIVERSITY (United States)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0000662623 PISSN: 00404039 EISSN: None Source Type: Journal
DOI: 10.1016/S0040-4039(00)95913-6 Document Type: Article

Times cited : (24)

References (18)

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2
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- Sundararaman¹ Herz²

3
- 0006488342
- Oxidative rearrangements of various sorts have also been utilized to effect 1,3 enone transpositions. For a brief survey of these see
- (1975) J. Am. Chem. Soc. , vol.97 , pp. 4018
- Trost¹ Shanton²

4
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- (1975) J. Am. Chem. Soc. , vol.97 , pp. 5873
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5
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- Sharpless¹ Lauer²

6
- 0009276253
- Allylic sulfoxides. Useful intermediates in organic synthesis
- (1974) Accounts of Chemical Research , vol.6 , pp. 147
- Evans¹ Andrews²

7
- 37049123267
- Self-immolative asymmetric synthesis in the allylic rearrangement of an optically active amine oxide
- (1970) Journal of the Chemical Society D: Chemical Communications , pp. 419
- Moriwaki¹ Sawada² Inoyue³

8
- 0006008336
- (1961) J. Org. Chem. , vol.26 , pp. 3615
- Wharton¹ Bohler²

9
- 0000791953
- Acidities of sulfoximines and related oxosulfonium cations. Cyclopropyl effects and structures of .alpha.-sulfonyl-type carbanions
- (1980) The Journal of Organic Chemistry , vol.45 , pp. 3884
- Liotta¹ Zima²

10
- 0001632904
- (1982) J. Org. Chem. , vol.47 , pp. 1258
- Liotta¹ Zima² Saindane³

11
- 33947084958
- (1973) J. Org. Chem. , vol.38 , pp. 1775
- Stork¹ Danheiser²

12
- 2042524507
- (1979) Tetrahedron Lett. , pp. 399
- Corey¹ Schmidt²

13
- 0000533351
- (1980) Tetrahedron Lett. , pp. 731
- Corey¹ Schmidt²

14
- 0001632904
- (1982) J. Org. Chem. , vol.47 , pp. 1258
- Liotta¹ Saindane² Sunay³ Jamison⁴ Grossman⁵ Phillips⁶

15
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- For studies involving the use of PCC as an oxidant, see:
- (1975) Tetrahedron Lett. , pp. 2644
- Corey¹ Suggs²

16
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- (1975) J. Org. Chem. , vol.40 , pp. 2554
- Corey¹ Suggs²

17
- 84919070317
- Compounds 1 and 4 were prepared by addition of lithium acetylide 7 to propenyl methyl ketone and methyl vinyl ketone, respectively (vide infra).

18
- 84919070316
- The structure of ketone 3 was unequivocally established by independent synthesis.

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