1.
Org Lett
; 3(12): 1905-8, 2001 Jun 14.
Article
in English
| MEDLINE
| ID: mdl-11405741
ABSTRACT
[see reaction]. The reaction of activated alkynes with carbonyl compounds in the presence of a catalytic amount of a nucleophile leads to enol-protected functionalized propargyl alcohols and 1,3-dioxolane compounds by way of a mild carbon-carbon bond formation reaction.
2.
Org Lett
; 2(22): 3513-5, 2000 Nov 02.
Article
in English
| MEDLINE
| ID: mdl-11082022
ABSTRACT
[reaction: see text] A remarkable exo-facial template effect exercised by a 2, 3-O-isopropylidene protective group is the key for the entire 2, 3-trans stereoselectivity observed in the allylsilane addition promoted by BF(3).OEt(2) to 2,3-O-isopropylidene-protected pyrrolidines.
Subject(s)
Pyrrolidines/chemical synthesis , Drug Design , Imines , Indicators and Reagents , Molecular Conformation , Molecular Structure , Stereoisomerism
3.
Angew Chem Int Ed Engl
; 39(15): 2727-2729, 2000 Aug 04.
Article
in English
| MEDLINE
| ID: mdl-10934407