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AN ENANTIOSELECTIVE ROUTE TO CIS-2-(HYDROXYMETHYL)-5-ALKYLPYRROLIDINES AND TRANS-2-(HYDROXYMETHYL)-5-ALKYLPYRROLIDINES
Uppsala University.
Uppsala University.
Uppsala University.
1995 (English)In: JOURNAL OF ORGANIC CHEMISTRY, Vol. 60, no 19, 6091-6096 p.Other (Other scientific)
Abstract [en]

A general method for the enantioselective preparation of 2,5-disubstituted pyrrolidines has been developed. A variety of cis- and trans-2-(hydroxymethyl)-5-alkylpyrrolidin were synthesized using 1-(benzyloxy)-5-(p-toluenesulfonamido)-3-alken-2-ol as comm

Place, publisher, year, pages
AMER CHEMICAL SOC , 1995. Vol. 60, no 19, 6091-6096 p.
Keyword [en]
STEREOCONTROLLED ORGANOPALLADIUM ROUTE; CHIRAL AUXILIARY; DERIVATIVES; ALCOHOLS; ALKYLATION; NMR; 1;4-ACETOXYCHLORINATION; 1;3-DIENES; INDUCTION; ALKALOIDS
Identifiers
URN: urn:nbn:se:uu:diva-68460OAI: oai:DiVA.org:uu-68460DiVA: diva2:96371
Note
Addresses: UNIV UPPSALA, DEPT ORGAN CHEM, S-75121 UPPSALA, SWEDEN.Available from: 2008-10-17 Created: 2008-10-17

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