Influence of the N-MOM group in the enantioselective lipase catalyzed methanolysis of racemic 1,4-dihydropyridine dicarboxylates

Tetrahedron Asymmetry

Volumn 8, Issue 6, 1997, Pages 857-858

  Soledad De Castro, M ^a   Salazar, Loreto ^a   Sinisterra, José V ^a  

^a UNIVERSIDAD COMPLUTENSE DE MADRID   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

1,4 DIHYDROPYRIDINE DERIVATIVE; TRIACYLGLYCEROL LIPASE;

ARTICLE; CATALYSIS; DRUG SYNTHESIS; ENZYME ACTIVE SITE; HYDROLYSIS; PRIORITY JOURNAL; PSEUDOMONAS; REACTION ANALYSIS; STEREOSPECIFICITY;

EID: 0030958196     PISSN: 09574166     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0957-4166(97)00043-8     Document Type: Article

References (7)

1. a) Holdgrün, X. K.; Sih, C. J. Tetrahedron Letters 1991, 32, 3465-3468;
2. b) Ebiike, H.; Terao, Y.; Achiwa, K.; Tetrahedron Letters, 1991, 32, 5805-5808;
3. c) Hirose, Y.; Kariya, K.; Sasaki, Y.; Kurono, Y.; Ebiike, H.; Achiwa, K. Tetrahedron Letters, 1992, 33, 7157-7160.
4. Salazar, L.; Sih, C. J. Tetrahedron: Asymmetry, 1995, 6, 2917-2920.
5. Compounds 3a-b were synthesized by known methods: a) Murakami, M.; Takahashi, K.; Osaza, T.; Tamazawa, K.; Kawai, R.; Takanaza, T. Japanese Patent (kokai), 1973, 85574;
6. b) Ogawa, T.; Nakazato, A.; Tsuchida, K.; Hatayama, K. Chem. Pharm. Bull., 1993, 41, 108-116.
7. 3. The absolute configuration was determined by analogy with known optically active compounds (Ref. 3).