Calculated conformations of sialyl-Lex- and sialyl-Lea-lactones

Ulf Ellervik; Göran Magnusson

doi:10.1016/S0968-0896(00)82077-5

Calculated conformations of sialyl-Lex- and sialyl-Lea-lactones

Ulf Ellervik, Göran Magnusson

Lunds Tekniska Högskola

Forskningsoutput: Tidskriftsbidrag › Artikel i vetenskaplig tidskrift › Peer review

Sammanfattning

The minimum energy conformations of the four sterically reasonable SLex and SLea lactones were calculated using the molecular mechanics force-field MM2(91). The tetrasaccharide lactone involving the 3- and 2-position of the Gal moiety was found to be more stable than the 3,4-lactone both for SLex and SLea. © 1994.

Originalspråk	engelska
Sidor (från-till)	1261-1266
Tidskrift	Bioorganic and Medicinal Chemistry
Volym	2
Nummer	11
DOI	https://doi.org/10.1016/S0968-0896(00)82077-5
Status	Published - 1994

Ämnesklassifikation (UKÄ)

Organisk kemi

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10.1016/S0968-0896(00)82077-5

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@article{727897049db048ceade8bcd234927350,

title = "Calculated conformations of sialyl-Lex- and sialyl-Lea-lactones",

abstract = "The minimum energy conformations of the four sterically reasonable SLex and SLea lactones were calculated using the molecular mechanics force-field MM2(91). The tetrasaccharide lactone involving the 3- and 2-position of the Gal moiety was found to be more stable than the 3,4-lactone both for SLex and SLea. {\textcopyright} 1994.",

author = "Ulf Ellervik and G{\"o}ran Magnusson",

year = "1994",

doi = "10.1016/S0968-0896(00)82077-5",

language = "English",

volume = "2",

pages = "1261--1266",

journal = "Bioorganic and Medicinal Chemistry",

issn = "0968-0896",

publisher = "Elsevier",

number = "11",

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TY - JOUR

T1 - Calculated conformations of sialyl-Lex- and sialyl-Lea-lactones

AU - Ellervik, Ulf

AU - Magnusson, Göran

PY - 1994

Y1 - 1994

N2 - The minimum energy conformations of the four sterically reasonable SLex and SLea lactones were calculated using the molecular mechanics force-field MM2(91). The tetrasaccharide lactone involving the 3- and 2-position of the Gal moiety was found to be more stable than the 3,4-lactone both for SLex and SLea. © 1994.

AB - The minimum energy conformations of the four sterically reasonable SLex and SLea lactones were calculated using the molecular mechanics force-field MM2(91). The tetrasaccharide lactone involving the 3- and 2-position of the Gal moiety was found to be more stable than the 3,4-lactone both for SLex and SLea. © 1994.

U2 - 10.1016/S0968-0896(00)82077-5

DO - 10.1016/S0968-0896(00)82077-5

M3 - Article

SN - 0968-0896

VL - 2

SP - 1261

EP - 1266

JO - Bioorganic and Medicinal Chemistry

JF - Bioorganic and Medicinal Chemistry

IS - 11

ER -

Calculated conformations of sialyl-Lex- and sialyl-Lea-lactones

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Ämnesklassifikation (UKÄ)

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