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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Synthesis of alpha-chloroacetophenones with NH4Cl/Oxone (R) in situ followed by bioreduction with whole cells of marine-derived fungi

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Author(s):
Morais, Aline T. do B. [1] ; Ferreira, Irlon M. [2] ; Jimenez, David E. Q. [1] ; Porto, Andre L. M. [1]
Total Authors: 4
Affiliation:
[1] Univ Sao Paulo, Inst Quim Sao Carlos, Lab Quim Organ & Biocatalise, Ave Joao Dagnone, 1100, Ed Quim Ambiental, BR-13563120 Sao Carlos, SP - Brazil
[2] Univ Fed Amapa, Colegiado Quim, Grp Biocatalise & Biotransformacao Quim Organ, Rod Juscelino Kubitschek, Km 2, BR-68902280 Macapa, AP - Brazil
Total Affiliations: 2
Document type: Journal article
Source: BIOCATALYSIS AND AGRICULTURAL BIOTECHNOLOGY; v. 16, p. 314-319, OCT 2018.
Web of Science Citations: 1
Abstract

Chiral chlorohydrins are used as intermediates in the synthesis of various compounds with biological activities. This paper reports the synthesis of alpha-chloroketones 2a-c with oxone (R) and NH4Cl at reflux via 30 min of exposure to microwave irradiation and conventional heating, in situ, followed by reduction with whole cells of marine-derived fungi (Penicillium citrinum CBMAI 1186, Mucor racemosus CBMAI 847, Aspergillus sydowii CBMAI 935, Penicillium raistrickii CBMAI 931, and Penicillium oxalicum CBMAI 1185), yielding the respective chlorohydrins 3a-c with good conversion (32-97%) and enantioselectivities (60-94%). This is the first study involving the synthesis of alpha-chlorophenones in situ followed by biocatalytic reduction from whole cells of marine-derived fungi to obtain enantio-enriched chlorohydrins 3a-c. (AU)

FAPESP's process: 13/50201-2 - Biodegrading of the organophosphate pesticide profenofós by marine fungi
Grantee:Andre Luiz Meleiro Porto
Support Opportunities: Regular Research Grants - Publications - Books published abroad