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An enantioselective synthesis of (+)-pseudohygroline.
Uppsala University.
Uppsala University.
Uppsala University.
Uppsala University.
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1998 (English)In: TETRAHEDRON LETTERS, Vol. 39, no 18, 2813-2814 p.Other (Other scientific)
Abstract [en]

The enantioselective synthesis of (+)-pseudohygroline (3), employing a highly diastereoselective ring closure as a key step, has been achieved in seven steps from readily available protected lactaldehyde (6). (C) 1998 Elsevier Science Ltd. All rights res

Place, publisher, year, pages
PERGAMON-ELSEVIER SCIENCE LTD , 1998. Vol. 39, no 18, 2813-2814 p.
Keyword [en]
INTRAMOLECULAR OXYMERCURATIONS
Identifiers
URN: urn:nbn:se:uu:diva-84781OAI: oai:DiVA.org:uu-84781DiVA: diva2:112689
Note
Addresses: Perlmutter P, Monash Univ, Dept Chem, Clayton, Vic 3168, Australia. Monash Univ, Dept Chem, Clayton, Vic 3168, Australia. Australian Natl Univ, Res Sch Chem, Acton, ACT 0200, Australia. Uppsala Univ, Dept Organ Chem, Uppsala, Sweden.Available from: 2008-10-17 Created: 2008-10-17

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