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Rotamers in Crystal Structures of Xylitol, D-Arabitol and L-Arabitol

Rotamers in Crystal Structures of Xylitol, D-Arabitol and L-Arabitol

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8998848

Rotamers in Crystal Structures of Xylitol, D-Arabitol and L-Arabitol

About this item

Full title

Rotamers in Crystal Structures of Xylitol, D-Arabitol and L-Arabitol

Publisher

Switzerland: MDPI AG

Journal title

International journal of molecular sciences, 2022-03, Vol.23 (7), p.3875

Language

English

Formats

Publication information

Publisher

Switzerland: MDPI AG

More information

Scope and Contents

Contents

Rotamers are stereoisomers produced by rotation (twisting) about σ bonds and are often rapidly interconverting at room temperature. Xylitol—massively produced sweetener—(2R,3r,4S)-pentane-1,2,3,4,5-pentol) forms rotamers from the linear conformer by rotation of a xylitol fragment around the C2–C3 bond (rotamer 1) or the C3–C4 bond (rotamer 2). The...

Alternative Titles

Full title

Rotamers in Crystal Structures of Xylitol, D-Arabitol and L-Arabitol

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8998848

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8998848

Other Identifiers

ISSN

1422-0067,1661-6596

E-ISSN

1422-0067

DOI

10.3390/ijms23073875

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