Detalhes bibliográficos
Ano de defesa: |
2012 |
Autor(a) principal: |
SIQUEIRA, Edmilson Clarindo de
 |
Orientador(a): |
DOBOSZEWSKI, Bogdan |
Banca de defesa: |
FREITAS FILHO, João Rufino de,
ANTUNES, Roberto de Vasconcelos,
HALLWASS, Fernando |
Tipo de documento: |
Dissertação
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Tipo de acesso: |
Acesso aberto |
Idioma: |
por |
Instituição de defesa: |
Universidade Federal Rural de Pernambuco
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Programa de Pós-Graduação: |
Programa de Pós-Graduação em Química
|
Departamento: |
Departamento de Química
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País: |
Brasil
|
Palavras-chave em Português: |
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Palavras-chave em Inglês: |
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Área do conhecimento CNPq: |
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Link de acesso: |
http://www.tede2.ufrpe.br:8080/tede2/handle/tede2/6329
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Resumo: |
In this study we investigated the resolution of rac-1,2-propanediol and rac-2,3- isopropylidene glycerol using chiral amines (R)- and (S)-1-phenylethylamine (27). The alcohols are esterified to form hemi-phthalates, and treated with the enantiomers of 27 resulting in the following salts (R)-27.(±)-52 and (S)-27.(±)-52 in good yields. However, salts (R)-27.(±)-33 and (S)-27.(±)-33 did not form crystalline material. In addition we studied the resolution of (±)-14 and (±)-31 through the use of amino acids benzyl esters and brucine as auxiliaries. Attempts to obtain the benzyl ester of L-tryptophan (59) were negative; attempts to obtain benzyl esters of Lphenylalanine (58) and L-lysine (57) were also negative. In the case of brucine (35) there was no noticeable diastereoisomeric enrichment during repeated crystallizations. As an extension to this, we performed dehydration of D-mannitol (40) in an acid medium. Modifications of the published method resulted in obtaining a new derivative, the 2,5-anhydro-1,3-O-benzyl-D-mannitol (81) whose structure was established via x-ray study. |