SCOPUS 정보 검색 플랫폼 - 논문 보기

메뉴 건너뛰기

Tetrahedron Letters

Volumn 22, Issue 14, 1981, Pages 1283-1286

Direct α-hydroxylation of ketones using iodosobenzene

(3) Moriarty, Robert M a Hu, Henry a Gupta, Satish C a

a UNIVERSITY OF ILLINOIS AT CHICAGO (United States)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0001148133 PISSN: 00404039 EISSN: None Source Type: Journal
DOI: 10.1016/S0040-4039(01)90297-7 Document Type: Article

Times cited : (190)

References (35)

1
- 37049047158
- 307. Compounds related to the steroid hormones. Part IX. Oxygenation of steroid ketones in strongly basic medium: a new method of preparation of 17?-hydroxypregnan-20-ones
- (1962) Journal of the Chemical Society (Resumed) , pp. 1578
- Bailey¹ Barton² Elks³ Templeton⁴

2
- 0002281603
- (1967) Bull. Soc. Chim. Fr. , pp. 3742
- Hanna¹ Ourisson²

3
- 0002316527
- (1961) Bull. Soc. Chim. Fr. , pp. 1945
- Hanna¹ Ourisson²

4
- 0014405157
- (1968) J. Amer. Chem. Soc. , vol.90 , pp. 6534
- Muxfeldt¹ Hardtmann² Kathawala³ Vedejs⁴ Mooberty⁵

5
- 0014428433
- Total synthesis of velbanamine
- (1968) Journal of the American Chemical Society , vol.90 , pp. 2448
- Büchi¹ Kulsa² Rosati³

6
- 0141825208
- Oxidation products of ethyl .alpha.-safranate
- (1972) The Journal of Organic Chemistry , vol.37 , pp. 4192
- Büchi¹ Pickenhagen² Wuest³

7
- 0343143075
- (1963) J. Amer. Chem. Soc. , vol.85 , pp. 1655
- Avramoff¹ Sprinzak²

8
- 37049045490
- (1962) Proc. Chem. Soc., London , pp. 279
- Gersmann¹ Nieuwenhuis² Bickel³

9
- 0014322443
- (1968) J. Org. Chem. , vol.33 , pp. 3294
- Gardner¹ Carlson² Gnoj³

10
- 84918330552
- 2 passing through resulted in a sudden powerful explosion.

11
- 33947092680
- (1978) J. Org. Chem. , vol.43 , pp. 188
- Vedejs¹ Engler² Telschow³

12
- 0000626006
- (1974) Tetrahedron Lett. , pp. 4319
- Rubottom¹ Vazquez² Pelegrina³

13
- 84918653188
- Synthetic methods. VIII. Hydroxylation of carbonyl compounds via silyl enol ethers
- (1975) The Journal of Organic Chemistry , vol.10 , pp. 3427
- Hassner¹ Reuss² Pinnick³

14
- 0001574139
- (1975) J. Org. Chem. , vol.40 , pp. 3783
- Rubottom¹ Marrero²

15
- 37049100023
- Synthesis of macrocyclic compounds containing the ferrocene unit
- (1980) Journal of the Chemical Society, Chemical Communications , pp. 163
- Bell¹ Hall²

16
- 84918330551
- Phenyliodosodiacetate may also be used, but in this case 3 moles of base are required.

17
- 84918318759
- J. Chem. Soc.
- (1972) J. Chem. Soc. , pp. 244
- Robertson¹ Robinson²

18
- 0009503160
- (1906) Ber. , vol.39 , pp. 3761
- Auwers¹

19
- 84913996556
- (1910) Comptes Rendus , vol.150 , pp. 1182
- Tiffeneau¹

20
- 84918330550
- + 154;

21
- 4043130724
- THE IDENTIFICATION OF ACIDS. V. PARA HALOGEN PHENACYL ESTERS.
- (1920) Journal of the American Chemical Society , vol.42 , pp. 1054
- Judefind¹ Reid²

22
- 0012196199
- (1887) Ber. , vol.22 , pp. 204
- Engler¹ Zielke²

23
- 84918330549
- The dimethylketal may be isolated and converted to the acyloin using p-TsOH/acetone or acid may be used in the work-up of the original reaction.

24
- 3242816558
- (1965) Zh. Org. Khim. , vol.1 , pp. 1854
- Neilands¹ Karele²

25
- 0011294083
- (1966) Zh. Org. Khim. , vol.2 , pp. 488
- Neilands¹ Karele²

26
- 0000545605
- (1971) Zh. Org. Khim. , vol.7 , pp. 1611
- Neilands¹ Karele²

27
- 0345005500
- Desyl chloride, upon reaction with methoxide yields the methoxyether.
- (1953) J. Am. Chem. Soc. , vol.75 , pp. 3977
- Stevens¹ Weiner² Freeman³

28
- 0007631397
- (1978) J. Am. Chem. Soc. , vol.100 , pp. 4888
- Reich¹ Peake²

29
- 37049108810
- Oxidative displacement of hypervalent iodine from alkyl iodides
- (1980) Journal of the Chemical Society, Perkin Transactions 1 , pp. 822
- Cambie¹ Chambers² Lindsay³ Rutledge⁴ Woodgate⁵

30
- 84918330548
- 2-) 8.10 ~ 8.25 (3H, pyridinium) IR [[Truncated]]

31
- 0345005500
- Deoxybenzoin yields 1,2-diphenyl-1-methoxyethylene oxide (53% yield).
- (1953) J. Am. Chem. Soc. , vol.75 , pp. 3977
- Stevens¹ Weiner² Freeman³

32
- 84918330547
- −1.

33
- 84918330546
- −1.

34
- 84918330545
- α-Hydroxypropiophenone was obtained in 75% yield
- (1917) Ber. , vol.50 , pp. 1179
- Auwers¹

35
- 0000498692
- 1,3-Diphenyl-2-hydroxy-1-propanone was obtained in 80% yield, This is formally a rearrangement product in relationship to the expected 1,3-diphenyl-1-hydroxy-2-propanone. Base equilibration between these isomers is discussed by Julian et al. vide infra..
- (1945) J. Am. Chem. Soc. , vol.67 , pp. 1203
- Julian¹ Meyer² Magnani³ Cole⁴

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.