{"id":{"repo_id":"wfu","oai_identifier":"oai:wakespace.lib.wfu.edu:10339/30428"},"canonical_url":"https://search.dev.ndltd.org/etd/wfu/oai:wakespace.lib.wfu.edu:10339/30428","repository":{"repo_id":"wfu","name":"Wake Forest University","base_url":"https://wakespace.lib.wfu.edu/oai/request"},"display":{"title":"DEVELOPMENT OF SYNTHETIC METHODOLOGIES TOWARDS CYCLIC HYDROXAMIC ACID-BASED NATURAL PRODUCTS","abstract":"Hydroxamic acids are an important class of bioactive compounds with wide uses as anti-bacterial, or anti-inflammatory agents and a key component of many natural products, mainly siderophores (low-molecular-weight iron sequestering agents) in lower organisms. Hydroxamic acid based analogs may find potential therapeutic uses in the inhibition of siderophore biosynthesis. Our research targets to develop new synthetic methodology towards making cyclic hydroxamic acids in a stereoselective and regioselective fashion. Basic decomposition of Piloty's acid transforms cyclic ketones (mainly four and five membered) into ring-expanded cyclic hydroxamic acids in 20-69% yield (Scheme 1). Mechanistic study reveals this reaction involves a C-nitroso intermediate 98 (Scheme 47) in the course of the rearrangement, which can also be generated by a separate hydrolysis reaction of acyloxy nitroso intermediate 103 (Scheme 51) leading to the ring-expansion product in 75-80% yield.","abstract_html":"Hydroxamic acids are an important class of bioactive compounds with wide uses as anti-bacterial, or anti-inflammatory agents and a key component of many natural products, mainly siderophores (low-molecular-weight iron sequestering agents) in lower organisms. Hydroxamic acid based analogs may find potential therapeutic uses in the inhibition of siderophore biosynthesis. Our research targets to develop new synthetic methodology towards making cyclic hydroxamic acids in a stereoselective and regioselective fashion. Basic decomposition of Piloty's acid transforms cyclic ketones (mainly four and five membered) into ring-expanded cyclic hydroxamic acids in 20-69% yield (Scheme 1). Mechanistic study reveals this reaction involves a C-nitroso intermediate 98 (Scheme 47) in the course of the rearrangement, which can also be generated by a separate hydrolysis reaction of acyloxy nitroso intermediate 103 (Scheme 51) leading to the ring-expansion product in 75-80% yield.","abstract_has_math":false,"creators":["Banerjee, Ranjan"],"institution":"Wake Forest University","degree_name":null,"degree_level":null,"degree_discipline":null,"degree_department":null,"school":null,"contributors":[],"advisors":[],"committee_chairs":[],"committee_members":[],"year":2010,"date_issued":"2010","date_published":"2010","updated_at":"2026-07-27T22:01:14Z","subjects":["Cobactine and Mycobactic Acid"],"languages":["en"],"rights":[],"rights_urls":[],"identifier_entries":[]},"links":{"outbound_url":"http://hdl.handle.net/10339/30428","outbound_label":"Handle","outbound_source":"dc:identifier.uri"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:creator","label":"Author","values":["Banerjee, Ranjan"]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"dc:date.accessioned","label":"Dc Date Accessioned","values":["2011-02-16T21:42:36Z"]},{"key":"dc:date.available","label":"Dc Date Available","values":["2012-12-14T09:30:08Z"]},{"key":"dc:date.issued","label":"Date","values":["2010"]},{"key":"dc:publisher","label":"Institution","values":["Wake Forest University"]},{"key":"dc:type","label":"Dc Type","values":["Dissertation"]}]},{"id":"subjects_keywords","label":"Subjects and Keywords","entries":[{"key":"dc:subject","label":"Dc Subject","values":["Cobactine and Mycobactic Acid"]}]},{"id":"language_rights","label":"Language and Rights","entries":[{"key":"dc:language.iso","label":"Language (ISO)","values":["en"]}]},{"id":"identifiers","label":"Identifiers","entries":[{"key":"dc:identifier.uri","label":"Identifier URI","values":["http://hdl.handle.net/10339/30428"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description.abstract","label":"Abstract","values":["Hydroxamic acids are an important class of bioactive compounds with wide uses as anti-bacterial, or anti-inflammatory agents and a key component of many natural products, mainly siderophores (low-molecular-weight iron sequestering agents) in lower organisms. Hydroxamic acid based analogs may find potential therapeutic uses in the inhibition of siderophore biosynthesis. Our research targets to develop new synthetic methodology towards making cyclic hydroxamic acids in a stereoselective and regioselective fashion. Basic decomposition of Piloty's acid transforms cyclic ketones (mainly four and five membered) into ring-expanded cyclic hydroxamic acids in 20-69% yield (Scheme 1). Mechanistic study reveals this reaction involves a C-nitroso intermediate 98 (Scheme 47) in the course of the rearrangement, which can also be generated by a separate hydrolysis reaction of acyloxy nitroso intermediate 103 (Scheme 51) leading to the ring-expansion product in 75-80% yield."]},{"key":"dc:title","label":"Title","values":["DEVELOPMENT OF SYNTHETIC METHODOLOGIES TOWARDS CYCLIC HYDROXAMIC ACID-BASED NATURAL PRODUCTS"]}]}],"canonical_facts":{"dc:creator":["Banerjee, Ranjan"],"dc:date.accessioned":["2011-02-16T21:42:36Z"],"dc:date.available":["2012-12-14T09:30:08Z"],"dc:date.issued":["2010"],"dc:description.abstract":["Hydroxamic acids are an important class of bioactive compounds with wide uses as anti-bacterial, or anti-inflammatory agents and a key component of many natural products, mainly siderophores (low-molecular-weight iron sequestering agents) in lower organisms. Hydroxamic acid based analogs may find potential therapeutic uses in the inhibition of siderophore biosynthesis. Our research targets to develop new synthetic methodology towards making cyclic hydroxamic acids in a stereoselective and regioselective fashion. Basic decomposition of Piloty's acid transforms cyclic ketones (mainly four and five membered) into ring-expanded cyclic hydroxamic acids in 20-69% yield (Scheme 1). Mechanistic study reveals this reaction involves a C-nitroso intermediate 98 (Scheme 47) in the course of the rearrangement, which can also be generated by a separate hydrolysis reaction of acyloxy nitroso intermediate 103 (Scheme 51) leading to the ring-expansion product in 75-80% yield."],"dc:identifier.uri":["http://hdl.handle.net/10339/30428"],"dc:language.iso":["en"],"dc:publisher":["Wake Forest University"],"dc:subject":["Cobactine and Mycobactic Acid"],"dc:title":["DEVELOPMENT OF SYNTHETIC METHODOLOGIES TOWARDS CYCLIC HYDROXAMIC ACID-BASED NATURAL PRODUCTS"],"dc:type":["Dissertation"]},"updated_at":"2026-07-27T22:01:14Z"}