Synthesis, stereochemistry and absolute configuration of deodarols and deodarones

Margarita B. Villecco; Luis R. Hernández; Marcelo I. Guzmán; César A.N. Catalán; María A. Bucio; Pedro Joseph-Nathan

doi:10.1016/S0957-4166(01)00521-3

Synthesis, stereochemistry and absolute configuration of deodarols and deodarones

Margarita B. Villecco
, Luis R. Hernández
, Marcelo I. Guzmán
, César A.N. Catalán
, María A. Bucio
, Pedro Joseph-Nathan

Producción científica: Article › revisión exhaustiva

3 Citas (Scopus)

Resumen

The stereochemistry and absolute configuration of the four deodarols 3 and two deodarones 4 derived from (R)-(+)-limonene 1 is described.

Idioma original	English
Páginas (desde-hasta)	2947-2953
Número de páginas	7
Publicación	Tetrahedron Asymmetry
Volumen	12
N.º	21
DOI	https://doi.org/10.1016/S0957-4166(01)00521-3
Estado	Published - nov 26 2001

Nota bibliográfica

Funding Information:
The work in Tucumán was supported by grants from CONICET (Argentina) and Consejo de Investigaciones de la Universidad Nacional de Tucumán (CIUNT). Partial financial support from CoNaCyT (México) and stimulating support from CYTED (Spain) is also acknowledged.

Financiación

The work in Tucumán was supported by grants from CONICET (Argentina) and Consejo de Investigaciones de la Universidad Nacional de Tucumán (CIUNT). Partial financial support from CoNaCyT (México) and stimulating support from CYTED (Spain) is also acknowledged.

Financiadores
Consejo Nacional de Investigaciones Científicas y Técnicas
Consejo Nacional de Ciencia, Tecnología e Innovación Tecnológica
Consejo de Investigación, Universidad Nacional de Salta
CYTED Ciencia y Tecnología para el Desarrollo

ASJC Scopus subject areas

Catalysis
Physical and Theoretical Chemistry
Organic Chemistry
Inorganic Chemistry

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10.1016/S0957-4166(01)00521-3

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title = "Synthesis, stereochemistry and absolute configuration of deodarols and deodarones",

abstract = "The stereochemistry and absolute configuration of the four deodarols 3 and two deodarones 4 derived from (R)-(+)-limonene 1 is described.",

author = "Villecco, \{Margarita B.\} and Hern{\'a}ndez, \{Luis R.\} and Guzm{\'a}n, \{Marcelo I.\} and Catal{\'a}n, \{C{\'e}sar A.N.\} and Bucio, \{Mar{\'i}a A.\} and Pedro Joseph-Nathan",

note = "Funding Information: The work in Tucum{\'a}n was supported by grants from CONICET (Argentina) and Consejo de Investigaciones de la Universidad Nacional de Tucum{\'a}n (CIUNT). Partial financial support from CoNaCyT (M{\'e}xico) and stimulating support from CYTED (Spain) is also acknowledged.",

year = "2001",

month = nov,

day = "26",

doi = "10.1016/S0957-4166(01)00521-3",

language = "English",

volume = "12",

pages = "2947--2953",

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T1 - Synthesis, stereochemistry and absolute configuration of deodarols and deodarones

AU - Villecco, Margarita B.

AU - Hernández, Luis R.

AU - Guzmán, Marcelo I.

AU - Catalán, César A.N.

AU - Bucio, María A.

AU - Joseph-Nathan, Pedro

N1 - Funding Information: The work in Tucumán was supported by grants from CONICET (Argentina) and Consejo de Investigaciones de la Universidad Nacional de Tucumán (CIUNT). Partial financial support from CoNaCyT (México) and stimulating support from CYTED (Spain) is also acknowledged.

PY - 2001/11/26

Y1 - 2001/11/26

N2 - The stereochemistry and absolute configuration of the four deodarols 3 and two deodarones 4 derived from (R)-(+)-limonene 1 is described.

AB - The stereochemistry and absolute configuration of the four deodarols 3 and two deodarones 4 derived from (R)-(+)-limonene 1 is described.

UR - https://www.scopus.com/pages/publications/0035956408

UR - https://www.scopus.com/pages/publications/0035956408#tab=citedBy

U2 - 10.1016/S0957-4166(01)00521-3

DO - 10.1016/S0957-4166(01)00521-3

M3 - Article

AN - SCOPUS:0035956408

SN - 0957-4166

VL - 12

SP - 2947

EP - 2953

JO - Tetrahedron Asymmetry

JF - Tetrahedron Asymmetry

IS - 21

ER -

Synthesis, stereochemistry and absolute configuration of deodarols and deodarones

Resumen

Nota bibliográfica

Financiación

ASJC Scopus subject areas

Acceder al documento

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