SCOPUS 정보 검색 플랫폼 - 논문 보기

메뉴 건너뛰기

Tetrahedron Letters

Volumn 27, Issue 49, 1986, Pages 5939-5942

The directed reduction of β-hydroxy ketones employing Me4NHB(OAc)3

(2) Evans, David A a Chapman, Kevin T a

a HARVARD UNIVERSITY (United States)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0000375471 PISSN: 00404039 EISSN: None Source Type: Journal
DOI: 10.1016/S0040-4039(00)85367-8 Document Type: Article

Times cited : (209)

References (20)

1
- 0021173293
- For earlier work on directed hydrogenation reactions see
- (1984) Tetrahedron Lett. , vol.25 , pp. 4637
- Evans¹ Morrissey²

2
- 0006141543
- (1984) J. Am. Chem. Soc. , vol.106 , pp. 3866
- Evans¹ Morrissey²

3
- 0000766635
- (1985) Tetrahedron Lett. , vol.26 , Issue.49 , pp. 6005
- Evans¹ Morrissey² Dow³

4
- 33845551063
- (1983) J. Am. Chem. Soc. , vol.105 , pp. 1072
- Stork¹ Kahne²

5
- 33845374498
- (1986) J. Org. Chem. , vol.51 , pp. 2655
- Crabtree¹ Davis²

6
- 84952187060
- For an excellent review of borohydride reductions in acidic media see ai]Gribble, G.W.
- (1983) Organic Preparation and Procedures Int. , vol.17 , pp. 317-384
- Nutaitis¹

7
- 0013548653
- (1983) Tetrahedron Lett. , vol.24 , pp. 4287
- Gribble¹ Nutaitis²

8
- 0020673714
- (1983) Tetrahedron Lett. , vol.24 , pp. 273
- Saksena¹ Mangiaracina²

9
- 0021678065
- (1984) Tetrahedron Lett. , vol.25 , pp. 5449
- Turnbull¹ Hatter² Ledgerwood³

10
- 84918457953
- In the above studies (Ref.4b, 5), the borohydride species were never fully characterized.

11
- 84918457952
- After a six-month period the reagent does not completely dissolve in solvents other than acetic acid. This does not, however, lead to a drop in reduction yield or stereoselectivity.

12
- 33947469085
- (1952) J. Am. Chem. Soc. , vol.74 , pp. 2346
- Banus¹ Bragdon² Gibb³

13
- 0344934872
- (1958) J. Inorg. Nucl. Chem. , vol.7 , pp. 404-411
- Wartik¹ Pearson²

14
- 0000473171
- (1975) J. Org. Chem. , vol.40 , pp. 3453
- Marchini¹ Liso² Reho³ Liberatore⁴ Moracci⁵

15
- 0019297509
- Chem. Abs. 94 1981 121481g
- (1980) Acta Pharm. Jugosl. , vol.30 , pp. 121
- Oklobdzija¹ Fajdiga² Kovak³ Zonno⁴ Sega⁵ Sunjic⁶

16
- 84918457951
- Satisfactory spectral data elemental analyses were obtained for all compounds reported.

17
- 37049091664
- Asymmetric reduction of aromatic ketones with reagents prepared from sodium borohydride and various carboxylic acids in the presence of 1,2:5,6-di-O-isopropylidene-?-D-glucofuranose
- For comparisons of reactivity of acyloxyalkoxy borohydrides see
- (1981) Journal of the Chemical Society, Perkin Transactions 1 , pp. 900
- Hirao¹ Itsuno² Owa³ Nagami⁴ Mochizuki⁵ Zoorov⁶ Niakahama⁷ Yamazaki⁸

18
- 30044436307
- (1982) Indian J. Chem. , vol.21 B , pp. 212-215
- Nasipuri¹ Sakar² Konar³ Ghosh⁴

19
- 37049089571
- The application of difunctional organosilicon compounds to organic synthesis; 1,3-asymmetric induction in the reduction of ?-hydroxy-ketones
- (1986) Journal of the Chemical Society, Chemical Communications , pp. 831-832
- Anwar¹ Davis²

20
- 84987466985
- Stereoselective Reduction of ?-Hydroxy-?-ketoesters
- and references reported therein
- (1986) Helvetica Chimica Acta , vol.69 , pp. 803-805
- Kathawala¹ Prager² Prasad³ Repic⁴ Shapiro⁵ Stabler⁶ Widler⁷

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.