Synthesis of methyl (R)-2-O-propargylglycerate, a precursor to analogues of the 2-O-alkylglycerate part of the moenomycins

Madina Mansourova; Katja Rohr; Lothar Hennig; Matthias Findeisen; Ramona Oehme; Sabine Giesa; Peter Welzel

doi:10.1002/ejoc.200300052

Synthesis of methyl (R)-2-O-propargylglycerate, a precursor to analogues of the 2-O-alkylglycerate part of the moenomycins

Madina Mansourova, Katja Rohr, Lothar Hennig, Matthias Findeisen, Ramona Oehme, Sabine Giesa, Peter Welzel

University of Leipzig

Producción científica: Contribución a una revista › Artículo › revisión exhaustiva

3 Citas (Scopus)

Resumen

Conditions allowing optically active methyl glycerate to be converted, without racemization, into the 2-O-propargyl derivative, via the 2-O-allyl derivative, are reported.

Idioma original	Inglés
Páginas (desde-hasta)	2656-2660
Número de páginas	5
Publicación	European Journal of Organic Chemistry
N.º	14
DOI	https://doi.org/10.1002/ejoc.200300052
Estado	Publicada - jul. 2003
Publicado de forma externa	Sí

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@article{4264d19847fd444fa58776856d960a94,

title = "Synthesis of methyl (R)-2-O-propargylglycerate, a precursor to analogues of the 2-O-alkylglycerate part of the moenomycins",

abstract = "Conditions allowing optically active methyl glycerate to be converted, without racemization, into the 2-O-propargyl derivative, via the 2-O-allyl derivative, are reported.",

keywords = "Alcohols, Alkynes, Allylation",

author = "Madina Mansourova and Katja Rohr and Lothar Hennig and Matthias Findeisen and Ramona Oehme and Sabine Giesa and Peter Welzel",

year = "2003",

month = jul,

doi = "10.1002/ejoc.200300052",

language = "English",

pages = "2656--2660",

journal = "European Journal of Organic Chemistry",

issn = "1434-193X",

number = "14",

}

TY - JOUR

T1 - Synthesis of methyl (R)-2-O-propargylglycerate, a precursor to analogues of the 2-O-alkylglycerate part of the moenomycins

AU - Mansourova, Madina

AU - Rohr, Katja

AU - Hennig, Lothar

AU - Findeisen, Matthias

AU - Oehme, Ramona

AU - Giesa, Sabine

AU - Welzel, Peter

PY - 2003/7

Y1 - 2003/7

N2 - Conditions allowing optically active methyl glycerate to be converted, without racemization, into the 2-O-propargyl derivative, via the 2-O-allyl derivative, are reported.

AB - Conditions allowing optically active methyl glycerate to be converted, without racemization, into the 2-O-propargyl derivative, via the 2-O-allyl derivative, are reported.

KW - Alcohols

KW - Alkynes

KW - Allylation

UR - https://www.scopus.com/pages/publications/0041344687

U2 - 10.1002/ejoc.200300052

DO - 10.1002/ejoc.200300052

M3 - Article

AN - SCOPUS:0041344687

SN - 1434-193X

SP - 2656

EP - 2660

JO - European Journal of Organic Chemistry

JF - European Journal of Organic Chemistry

IS - 14

ER -

Synthesis of methyl (R)-2-O-propargylglycerate, a precursor to analogues of the 2-O-alkylglycerate part of the moenomycins

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