WorldCat Identities

Bosch Cartes, Joan

Overview
Works: 60 works in 80 publications in 3 languages and 89 library holdings
Genres: Academic theses 
Roles: Translator, Author
Classifications: RS403, 547.1
Publication Timeline
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Most widely held works by Joan Bosch Cartes
Compendio esencial de química farmacéutica by Andrejus Korolkovas( Book )

3 editions published between 1978 and 1979 in Spanish and held by 9 WorldCat member libraries worldwide

Investigación de mecanismos de reacción en química orgánica by Peter Sykes( Book )

3 editions published between 1975 and 1985 in Spanish and Undetermined and held by 7 WorldCat member libraries worldwide

Estudio de 5-nitro-2-furil derivados y de sus productos de reducción by Joan Bosch Cartes( Book )

4 editions published between 1973 and 1974 in Spanish and held by 4 WorldCat member libraries worldwide

Síntesi d'anàlegs simplificats de l'alcaloide indòlic ervitsina by Jordi Bolós Gener( Book )

3 editions published in 1987 in Catalan and Spanish and held by 3 WorldCat member libraries worldwide

Síntesis de agonistas dopaminérgicos periféricos : 2-aminotetralinas y bioisósteros by Carlos-Gabriel Pérez Orcero( )

2 editions published between 1998 and 2019 in Spanish and held by 2 WorldCat member libraries worldwide

Se describe la síntesis de agonistas dopaminérgicos perifericos DA1/DA2, eficaces para el tratamiento de la insuficiencia cardiaca congestiva, en los que se ha sustituido la unidad de 2-aminotetralina caracteristica de este grupo de compuestos por un nucleo heteromatico bioisostero de catecolaminas, para superar los problemas de biodisponibilidad inherentes a la unidad de catecol. Para ello se ha establecido una vía de sintesis convergente, eficaz y de carácter general que ha permitido la preparación de estructuras de tipo 6-amino-2-hidroxitetrahidroquinolina, 6-aminotetrahidroquinolina, 3-piridiletilamina, 6-amino-2-hidroxitetrahidroquinolina, 6-aminotetrahidroquinolina, 3-piridiletilamina, 6-amino-2-hidroxitetrahidrobenzotiatol, 2,6-diaminotetrahidrobenzo-tiazol, 5-aminotetrahidroindol, 3-pirroliletilamina y 5-aminotetrahidroisoindol. Se han efectuado ensayos funcionales in vitro de actividad agonista dopaminérgica periferica de los compuestos sintetizados mediante el test de la arteria esplénica del conejo para la actividad DA1 y el test de la arteria auricular del conejo para la actividad DA2. Unicamente los compuestos de la serie tetrahidroquinolina actividad DA2 careciendo de actividad DA1, mientras que lo compuestos de la serie 2-aminotetrahidrobenzotiazol muestran actividad DA1 y DA2 aunque esta no es debida a una acción dopaminergica
Síntesi d'anàlegs dels 6,7-benzomorfans : 7,8-benzomorfans i b-norbenzomorfans by Montserrat Moral i Ajado( Book )

2 editions published in 1984 in Spanish and Catalan and held by 2 WorldCat member libraries worldwide

Estudios en la síntesis de alcaloides indolicos del tipo strychnos by Enric Sanfeliu i Soto( Book )

2 editions published in 1990 in Spanish and held by 2 WorldCat member libraries worldwide

5,6-dihidro-2(1H)-piridonas en la reacción de Diels-Alder: preparación y transformaciones sintéticas de octahidroisoquinolonas by Ángela Jorge Alesanco( )

3 editions published between 1998 and 2019 in Spanish and held by 2 WorldCat member libraries worldwide

La reacción de cicloadición de Diels-Alder entre 5,6-dihidro-2(1H)-piridonas como dienófilos y dienos convenientemente funcionalizados da lugar a la formación de sistemas bicíclicos de perhidroisoquinolona que pueden ser precursores de intermedios en la síntesis de numerosos compuestos naturales. En el presente trabajo se describe la preparación de diversas 5,6-dihidro-2(1H)-piridonas y se estudia su reactividad como dienófilos frente a diversos dienos y en diferentes condiciones experimentales. La posterior introducción de un grupo indolitetilo sobre el nitrógeno de las isoquinolinas obtenidas mediante esta metodología seguida de ciclación conduce a sistemas pentacíclicos de indolobenzoquinolizidina. Por otro lado, la ruptura oxidativa del doble enlace presente en el anillo no nitrogenado de la molécula de isoquinolona permite obtener núcleos de piperidonas sustituidas en las posiciones 3 y 4 con dos cadenas funcionalizadas. El anillo de piperidina 3,4 disustituida forma parte de la estructura de numerosos productos naturales como por ejemplo los alcaloides tetrahidrocantleyina, corinanteína o tubifolidina
Els quàdruplex de guanina estudis estructurals i diana farmacològica by Rubén Ferreira Aguilera( Book )

2 editions published in 2012 in Catalan and held by 2 WorldCat member libraries worldwide

Estudios sintéticos sobre estructuras tetracíclicas presentes en alcaloides indólico del tipo Strychnos by Ana Linares Obón( Book )

2 editions published in 1985 in Spanish and held by 2 WorldCat member libraries worldwide

[Nuevas vias para la síntesis de 2-azabiciclo (3.3.1) nonanos funcionalizados by Isabel Serret Melé( Book )

2 editions published between 1985 and 1986 in Spanish and held by 2 WorldCat member libraries worldwide

Fàrmacs de síntesi al segle XXI? discurs llegit a l'acte d'ingrés de l'acadèmic numerari Molt Il·lustre Dr. Joan Bosch Cartes, celebrat el dia 21 de juny de 2010 by Juan Bosch Cartes( Book )

2 editions published in 2010 in Catalan and held by 2 WorldCat member libraries worldwide

Open-chain building blocks from chiral lactams. Enantioselective synthesis of macrocyclic nitrogen-containing natural products by Guillaume Michel Pablo Guignard( Book )

2 editions published in 2016 in English and held by 2 WorldCat member libraries worldwide

1. (R)-Phenylglycinol-derived oxazolopiperidone lactams can be converted to enantiopure open-chain amino ester scaffolds by alkaline hydrolysis of the N-Boc 2-piperidones resulting from the reductive cleavage of the oxazolidine ring. 2. Lithium amidotrihydroborate (LiNH2BH3) reduction of diversely substituted (R)-phenylglycinol-derived oxazolopiperidone lactams brought about the reductive opening of both the oxazolidine and lactam rings, providing general access to structurally diverse enantiopure amino diols A bearing a variety of substitution patterns, substituents (alkyl, benzyl, aryl, protected hydroxy), and stereochemistries. 3. Reductive removal of the phenylethanol moiety present in the amino diols prepared by the above procedure, followed by treatment of the resulting primary amines with (Boc)2O provides a general synthetic entry to enantiopure N-Boc 5-aminopentanols bearing substitutents at the 2-, 3-, 4-, 2,2-, 2,3-, 2,4-, and 3,4- positions. 4. The oxidative removal of the phenylglycinol moiety of amino diols A (previously O-silylated) using the I2/aq NH3 system constitutes an excellent procedure for the straightforward preparation of enantiopure substituted 5-hydroxypentanenitrile derivatives. 5. The m-CPBA-promoted oxidative removal of the phenylglycinol moiety of amino diols A (previously O-silylated) constitutes an excellent procedure for the straightforward preparation of enantiopure substituted 5-hydroxypentanoic acid derivatives. 6. As both enantiomers of phenylglycinol are commercially available, both enantiomers of a target 5-aminopentanol, 5-hydroxypentanoic acid, and 5-hydroxypentanenitrile are accessible through the above methodology. 7. The synthetic value of the open-chain amino diols A has been demonstrated with their use as key scaffolds for the enantioselective synthesis of the Haliclona alkaloids haliclorensin C (first total synthesis), haliclorensin (total), halitulin (formal), and isohaliclorensin (formal). 8. The synthetic value of the open-chain amino diols 5-hydroxypentanoic acids, and 5-hydroxypentanenitriles prepared from (S)-phenylglycinol-derived lactams has been demonstrated with their use as key scaffolds for the synthesis of the natural macrolactam fluvirucinin B1. 9. The approach we have developed significantly expands the potential of phenylglycinol-derived d-lactams, which have been converted for the first time to enantiopure open-chain building blocks
Una nova metodologia en la síntesi dálcaloides indòlics pentacíclics del tipus strychnos :utilizació de 2-azabiziclo [3.3.1] nonam-7-ones by Núria Casamitjana( Book )

2 editions published in 1985 in Catalan and held by 2 WorldCat member libraries worldwide

Análogos pirrólicos de alcaloides indólicos : síntesis de pirrolo[2,3-g]morfanos y pirrolo [3,2-g]morfanos by Mercedes Amat Tusón( )

1 edition published in 1980 in Spanish and held by 1 WorldCat member library worldwide

Indolo [3,2-f] morfanos : problemas de síntesis by Dolors Pardo Llutart( )

1 edition published in 1980 in Spanish and held by 1 WorldCat member library worldwide

Primera síntesis total y reasignación estereoquímica del alcaloide indolico vinoxina by M. Lluïsa Bennasar Fèlix( )

1 edition published in 1984 in Spanish and held by 1 WorldCat member library worldwide

Síntesis de los alcaloides indolicos ngouniensina y epingouniensina by Ester Zulaica Gallego( )

1 edition published in 1987 in Spanish and held by 1 WorldCat member library worldwide

Síntesis de nuevas estructuras policíclicas que poseen la agrupación del 2-azabicilo[3.3.1] nonano by Rosa Andrés Moreno( )

1 edition published in 1981 in Spanish and held by 1 WorldCat member library worldwide

 
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Audience level: 0.91 (from 0.82 for Investigac ... to 0.97 for Síntesi d ...)

Alternative Names
Bosch Cartés, Joan

Bosch Cartes, Juan

Bosch i Cartes, Joan

Bosch, J.

Bosch, J. (Bosch Cartes)

Bosch, Joan

Bosch, Joan (Bosch Cartes)

Joan Bosch Cartes

Joan Bosch Cartes researcher

Joan Bosch onderzoeker

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