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Tetrahedron Letters

Volumn 29, Issue 39, 1988, Pages 4927-4930

Biocatalytic resolution of (±)-hydroxyalkanoic esters. A strategy for enhancing the enantiomeric specificity of lipase-catalyzed ester hydrolysis.

(3) Scilimati, A a Ngooi, T K a Sih, Charles J a

a UNIVERSITY OF WISCONSIN MADISON (United States)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0001498450 PISSN: 00404039 EISSN: None Source Type: Journal
DOI: 10.1016/S0040-4039(00)80643-7 Document Type: Article

Times cited : (56)

References (16)

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8
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9
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- (1988) Tetrahedron Lett. , vol.29 , pp. 423
- Flynn¹ Beight²

11
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12
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13
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- Microbial Asymmetric Catalysis?Enantioselective Reduction of Ketones [New Synthetic Methods (45)]
- Int. Ed. Engl.
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- Sih¹ Chen²

14
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- Syntheses of (3S, 4R, 15S)-4,15-Dimethyl-1,5-dioxa-3-(3′-formamidosalicylamido)-cyclopentadecane-2,6-dione and Its (15R)-Epimer, New Antimycin Analogs
- 3. The absolute configuration of the hydroxyalkanoic acids was made on the basis of the sign of optical rotation
- (1971) Bulletin of the Chemical Society of Japan , vol.44 , pp. 3395
- Kinoshita¹ Ishii² Umezawa³

15
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- The lipases AK and K-10 (Pseudomonas sp.) were products of Amano.

16
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- The enantiomeric ratio (E value) is calculated from:
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- Chen¹ Fujimoto² Girdaukas³ Sih⁴

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.