A Formal Synthesis of (-)-Brasilenol

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DC Field	Value	Language
dc.contributor.advisor	Kaliappan, Krishna	-
dc.contributor.author	CHAUHAN, TIRTH	-
dc.date.accessioned	2024-05-16T04:35:53Z	-
dc.date.available	2024-05-16T04:35:53Z	-
dc.date.issued	2024-05	-
dc.identifier.citation	48	en_US
dc.identifier.uri	http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/8789	-
dc.description.abstract	Our efforts towards a chiral pool synthesis of (-)-brasilenol from (-)-β-pinene is reported here. Starting from relatively abundant (-)-β-pinene, the unnatural enantiomer (-)-brasilenol was targeted in 11 steps. Use of stereospecific ring-opening was employed to ensure conservation of stereocenter at the isopropyl group, while hydrogenative stereospecific isomerization of exocyclic enone to endocyclic enone was utilized for prevention of racemization of the methyl group.	en_US
dc.description.sponsorship	DST INSPIRE	en_US
dc.language.iso	en	en_US
dc.subject	Natural Product	en_US
dc.subject	Formal Synthesis	en_US
dc.subject	Brasilenol	en_US
dc.subject	Chiral Pool	en_US
dc.title	A Formal Synthesis of (-)-Brasilenol	en_US
dc.title.alternative	A Formal Synthesis of (-)-Brasilenol from Chiral Pool	en_US
dc.type	Thesis	en_US
dc.description.embargo	One Year	en_US
dc.type.degree	BS-MS	en_US
dc.contributor.department	Dept. of Chemistry	en_US
dc.contributor.registration	20191159	en_US
Appears in Collections:	MS THESES

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