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Intramolecular amid...
Intramolecular amidomercurations under allylic control: a stereoselective synthesis of (+)-pseudohygroline and (+)-3-hydroxypyrrolizidine
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- Enierga, G (author)
- Uppsala universitet,Kemiska institutionen
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Espiritu, M (author)
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Perlmutter, P (author)
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Pham, N (author)
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Rose, M (author)
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Sjoberg, S (author)
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Thienthong, N (author)
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Wong, K (author)
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(creator_code:org_t)
- PERGAMON-ELSEVIER SCIENCE LTD, 2001
- 2001
- English.
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In: TETRAHEDRON-ASYMMETRY. - : PERGAMON-ELSEVIER SCIENCE LTD. - 0957-4166. ; 12:4, s. 597-604
- Related links:
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https://urn.kb.se/re...
Abstract
Subject headings
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- The diastereoselectivity of intramolecular amidomercurations can be reversed by altering the remote allylic substituent of omega -alkenylcarbamates. This methodology has been applied to the synthesis of (+)-pseudohygroline and (+)-3-hydroxypyrrolizidine.
Keyword
- OXYMERCURATIONS; ALKALOIDS
Publication and Content Type
- ref (subject category)
- art (subject category)
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