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beta-cyclodextrin-immobilized (4S)-phenoxy-(S)-proline as a catalyst for direct asymmetric aldol reactions.
Chirality. 2005 Nov; 17(9):556-8.C

Abstract

beta-Cyclodextrin-immobilized (4S)-phenoxy-(S)-proline was prepared conveniently by simply heating the amino acid and beta-cyclodextrin in ethanol-water (1/1, v/v) and removal of the solvent. This proved to be an efficient catalyst for direct asymmetric aldol reactions, and the catalyst could be recycled four times without loss of enantioselectivity.

Authors+Show Affiliations

Key Laboratory of Organic Synthesis of Jiangsu Province, College of Chemistry and Chemical Engineering, Suzhou University, Suzhou, China.No affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article

Language

eng

PubMed ID

16189836

Citation

Shen, Zongxuan, et al. "Beta-cyclodextrin-immobilized (4S)-phenoxy-(S)-proline as a Catalyst for Direct Asymmetric Aldol Reactions." Chirality, vol. 17, no. 9, 2005, pp. 556-8.
Shen Z, Ma J, Liu Y, et al. Beta-cyclodextrin-immobilized (4S)-phenoxy-(S)-proline as a catalyst for direct asymmetric aldol reactions. Chirality. 2005;17(9):556-8.
Shen, Z., Ma, J., Liu, Y., Jiao, C., Li, M., & Zhang, Y. (2005). Beta-cyclodextrin-immobilized (4S)-phenoxy-(S)-proline as a catalyst for direct asymmetric aldol reactions. Chirality, 17(9), 556-8.
Shen Z, et al. Beta-cyclodextrin-immobilized (4S)-phenoxy-(S)-proline as a Catalyst for Direct Asymmetric Aldol Reactions. Chirality. 2005;17(9):556-8. PubMed PMID: 16189836.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - beta-cyclodextrin-immobilized (4S)-phenoxy-(S)-proline as a catalyst for direct asymmetric aldol reactions. AU - Shen,Zongxuan, AU - Ma,Jimei, AU - Liu,Yanhua, AU - Jiao,Chongjun, AU - Li,Ming, AU - Zhang,Yawen, PY - 2005/9/29/pubmed PY - 2006/2/1/medline PY - 2005/9/29/entrez SP - 556 EP - 8 JF - Chirality JO - Chirality VL - 17 IS - 9 N2 - beta-Cyclodextrin-immobilized (4S)-phenoxy-(S)-proline was prepared conveniently by simply heating the amino acid and beta-cyclodextrin in ethanol-water (1/1, v/v) and removal of the solvent. This proved to be an efficient catalyst for direct asymmetric aldol reactions, and the catalyst could be recycled four times without loss of enantioselectivity. SN - 0899-0042 UR - https://www.unboundmedicine.com/medline/citation/16189836/beta_cyclodextrin_immobilized__4S__phenoxy__S__proline_as_a_catalyst_for_direct_asymmetric_aldol_reactions_ DB - PRIME DP - Unbound Medicine ER -