{"issue":"46","publisher":"Royal Society of Chemistry","pmid":1,"volume":57,"date_updated":"2026-02-20T07:01:01Z","has_accepted_license":"1","status":"public","day":"29","type":"journal_article","intvolume":" 57","extern":"1","date_published":"2021-04-29T00:00:00Z","external_id":{"pmid":["33972976 "]},"title":"Quantitative helix handedness bias through a single H vs. CH3 stereochemical differentiation","quality_controlled":"1","month":"04","oa_version":"None","author":[{"last_name":"Bindl","full_name":"Bindl, Daniel","first_name":"Daniel"},{"first_name":"Elisabeth","full_name":"Heinemann, Elisabeth","last_name":"Heinemann"},{"orcid":"0000-0001-5996-956X","full_name":"Mandal, Pradeep K","first_name":"Pradeep K","last_name":"Mandal","id":"6a3def15-d4b4-11ef-9fa9-a24c1f545ec3"},{"first_name":"Ivan","full_name":"Huc, Ivan","last_name":"Huc"}],"article_processing_charge":"No","article_type":"original","citation":{"ista":"Bindl D, Heinemann E, Mandal PK, Huc I. 2021. Quantitative helix handedness bias through a single H vs. CH3 stereochemical differentiation. Chemical Communications. 57(46), 5662–5665.","chicago":"Bindl, Daniel, Elisabeth Heinemann, Pradeep K Mandal, and Ivan Huc. “Quantitative Helix Handedness Bias through a Single H vs. CH3 Stereochemical Differentiation.” Chemical Communications. Royal Society of Chemistry, 2021. https://doi.org/10.1039/d1cc01452h.","apa":"Bindl, D., Heinemann, E., Mandal, P. K., & Huc, I. (2021). Quantitative helix handedness bias through a single H vs. CH3 stereochemical differentiation. Chemical Communications. Royal Society of Chemistry. https://doi.org/10.1039/d1cc01452h","short":"D. Bindl, E. Heinemann, P.K. Mandal, I. Huc, Chemical Communications 57 (2021) 5662–5665.","ieee":"D. Bindl, E. Heinemann, P. K. Mandal, and I. Huc, “Quantitative helix handedness bias through a single H vs. CH3 stereochemical differentiation,” Chemical Communications, vol. 57, no. 46. Royal Society of Chemistry, pp. 5662–5665, 2021.","ama":"Bindl D, Heinemann E, Mandal PK, Huc I. Quantitative helix handedness bias through a single H vs. CH3 stereochemical differentiation. Chemical Communications. 2021;57(46):5662-5665. doi:10.1039/d1cc01452h","mla":"Bindl, Daniel, et al. “Quantitative Helix Handedness Bias through a Single H vs. CH3 Stereochemical Differentiation.” Chemical Communications, vol. 57, no. 46, Royal Society of Chemistry, 2021, pp. 5662–65, doi:10.1039/d1cc01452h."},"abstract":[{"text":"A novel chiral aromatic δ-amino acid building block was shown to fully induce handedness in quinoline oligoamide foldamers with the possibility of further increasing the bias by combining multiples of these units in the same sequence. Through its incorporation within the helix, both N- and C-termini are still accessible for further functionalisation.","lang":"eng"}],"language":[{"iso":"eng"}],"doi":"10.1039/d1cc01452h","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","year":"2021","page":"5662-5665","publication_identifier":{"eissn":["1364-548X"],"issn":["1359-7345"]},"publication_status":"published","OA_type":"closed access","_id":"21082","date_created":"2026-01-29T15:18:02Z","publication":"Chemical Communications"}