Study of Chemical Ligation Via 17-, 18- and 19-Membered Cyclic Transition States

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dc.contributor.authorBajaj, Kiran
dc.date.accessioned2021-11-11T11:23:28Z
dc.date.available2021-11-11T11:23:28Z
dc.date.issued2012-09-14
dc.description.abstractUnprotected S-acylated cysteine isopeptides containing α-, β- or γ-amino acid units have been synthesized, and their conversion to native hexapeptides by S- to the N-terminus ligations involving 17-, 18- and 19-membered cyclic transition states have been demonstrated both experimentally and computationally to be more favorable than intermolecular cross-ligations.en_US
dc.identifier.urihttps://onlinelibrary.wiley.com/doi/10.1111/cbdd.12053
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3503
dc.language.isoenen_US
dc.publisherWileyen_US
dc.subjectChemistryen_US
dc.subjectChemical Ligationen_US
dc.subject19-Membered Cyclicen_US
dc.titleStudy of Chemical Ligation Via 17-, 18- and 19-Membered Cyclic Transition Statesen_US
dc.typeArticleen_US

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