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- Enierga, GUppsala universitet,Kemiska institutionen (author)
Intramolecular amidomercurations under allylic control: a stereoselective synthesis of (+)-pseudohygroline and (+)-3-hydroxypyrrolizidine
- Article/chapterEnglish2001
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- PERGAMON-ELSEVIER SCIENCE LTD,2001
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- LIBRIS-ID:oai:DiVA.org:uu-37628
- https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-37628URI
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- Language:English
- Summary in:English
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- Addresses: Perlmutter P, Monash Univ, Dept Chem, POB 23, Clayton, Vic 3800, Australia. Monash Univ, Dept Chem, Clayton, Vic 3800, Australia. Uppsala Univ, Dept Organ Chem, Uppsala, Sweden.
- 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.
Subject headings and genre
- OXYMERCURATIONS; ALKALOIDS
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- Espiritu, M (author)
- Perlmutter, P (author)
- Pham, N (author)
- Rose, M (author)
- Sjoberg, S (author)
- Thienthong, N (author)
- Wong, K (author)
- Uppsala universitetKemiska institutionen (creator_code:org_t)
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- In:TETRAHEDRON-ASYMMETRY: PERGAMON-ELSEVIER SCIENCE LTD12:4, s. 597-6040957-4166
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