Diastereoselective alkylation of chiral derivatives of acetoacetic acid

Marcial Moreno-Mañas; Rosa M. Sebastian; Adelina Vallribera; Elies Molins

doi:10.1016/0040-4020(95)00643-M

Diastereoselective alkylation of chiral derivatives of acetoacetic acid

Marcial Moreno-Mañas, Rosa M. Sebastian, Adelina Vallribera, Elies Molins

Departament de Química

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N-acetoacetyl-(S)-4-benzyloxazolidin-2-one and N-acctoacetyl-(R)-bornane-10,2-sultam are alkylated at the C-α of the acctoacetyl moiety with significant diastereoisomeric excesses. The diastereoisomers are in general easily separable and configurationally fairly stable. © 1995 Elsevier Science Ltd.

Idioma original	Anglès
Pàgines (de-a)	10795-10800
Revista	Tetrahedron
Volum	51
Número	39
DOIs	https://doi.org/10.1016/0040-4020(95)00643-M
Estat de la publicació	Publicada - 25 de set. 1995

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10.1016/0040-4020(95)00643-M

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title = "Diastereoselective alkylation of chiral derivatives of acetoacetic acid",

abstract = "N-acetoacetyl-(S)-4-benzyloxazolidin-2-one and N-acctoacetyl-(R)-bornane-10,2-sultam are alkylated at the C-α of the acctoacetyl moiety with significant diastereoisomeric excesses. The diastereoisomers are in general easily separable and configurationally fairly stable. {\textcopyright} 1995 Elsevier Science Ltd.",

author = "Marcial Moreno-Ma{\~n}as and Sebastian, \{Rosa M.\} and Adelina Vallribera and Elies Molins",

year = "1995",

month = sep,

day = "25",

doi = "10.1016/0040-4020(95)00643-M",

language = "English",

volume = "51",

pages = "10795--10800",

journal = "Tetrahedron",

issn = "0040-4020",

publisher = "Elsevier Limited",

number = "39",

}

TY - JOUR

T1 - Diastereoselective alkylation of chiral derivatives of acetoacetic acid

AU - Moreno-Mañas, Marcial

AU - Sebastian, Rosa M.

AU - Vallribera, Adelina

AU - Molins, Elies

PY - 1995/9/25

Y1 - 1995/9/25

N2 - N-acetoacetyl-(S)-4-benzyloxazolidin-2-one and N-acctoacetyl-(R)-bornane-10,2-sultam are alkylated at the C-α of the acctoacetyl moiety with significant diastereoisomeric excesses. The diastereoisomers are in general easily separable and configurationally fairly stable. © 1995 Elsevier Science Ltd.

AB - N-acetoacetyl-(S)-4-benzyloxazolidin-2-one and N-acctoacetyl-(R)-bornane-10,2-sultam are alkylated at the C-α of the acctoacetyl moiety with significant diastereoisomeric excesses. The diastereoisomers are in general easily separable and configurationally fairly stable. © 1995 Elsevier Science Ltd.

UR - https://www.scopus.com/pages/publications/0029029880

U2 - 10.1016/0040-4020(95)00643-M

DO - 10.1016/0040-4020(95)00643-M

M3 - Article

SN - 0040-4020

VL - 51

SP - 10795

EP - 10800

JO - Tetrahedron

JF - Tetrahedron

IS - 39

ER -

Diastereoselective alkylation of chiral derivatives of acetoacetic acid

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