Add to ORKGAn iodine-mediated ring closing alkene iodoamination with N-debenzylation protocol provides a direct route for the asymmetric synthesis of polyhydroxylated pyrrolidines from homochiral β-amino acid derivatives.</p
International audienceThe asymmetric synthesis of enantiopure pyrrolidines is reported via a streaml...
The synthesis of unusual cyclic amino acids, that may be envisaged as proline analogues, is an area ...
The asymmetric syntheses of 2,5-dideoxy-2,5-imino-d-glucitol [(+)-DGDP] and 1,2,5-trideoxy-1-amino-2...
Treatment of a range of homochiral unsaturated β-amino esters (containing a cis-dioxolane unit) with...
Ring-closing iodoamination of (E)-configured, N-α-methyl-p- methoxybenzyl protected homoallylic amin...
This thesis is concerned with the development of ring-closing iodoamination and ringexpansion method...
The functionalization of olefins induced by chiral hypervalent iodine reagents is a basic method for...
The transannular iodoamination of substituted 1,2,3,4,7,8-hexahydroazocine scaffolds has been develo...
[reaction: see text] A flexible route to polyhydroxylated pyrrolizidine alkaloids is described, star...
Thesis (Ph.D.)--University of Washington, 2012A plethora of natural products and valuable pharmaceut...
By detailed study of the possible side reactions in the previously reported aziridination of alkenes...
A new process has been developed for the selective construction of 2,6-disubstituted, 2,4,6-trisubst...
A thesis describing the asymmetric syntheses of three families of amino polyols. The asymmetric synt...
Summary: Metal-catalyzed reactions have revolutionized synthetic chemistry, allowing access to unpre...
This thesis describes approaches to bicyclic nitrogen heterocycles, similar to those found in the na...
International audienceThe asymmetric synthesis of enantiopure pyrrolidines is reported via a streaml...
The synthesis of unusual cyclic amino acids, that may be envisaged as proline analogues, is an area ...
The asymmetric syntheses of 2,5-dideoxy-2,5-imino-d-glucitol [(+)-DGDP] and 1,2,5-trideoxy-1-amino-2...
Treatment of a range of homochiral unsaturated β-amino esters (containing a cis-dioxolane unit) with...
Ring-closing iodoamination of (E)-configured, N-α-methyl-p- methoxybenzyl protected homoallylic amin...
This thesis is concerned with the development of ring-closing iodoamination and ringexpansion method...
The functionalization of olefins induced by chiral hypervalent iodine reagents is a basic method for...
The transannular iodoamination of substituted 1,2,3,4,7,8-hexahydroazocine scaffolds has been develo...
[reaction: see text] A flexible route to polyhydroxylated pyrrolizidine alkaloids is described, star...
Thesis (Ph.D.)--University of Washington, 2012A plethora of natural products and valuable pharmaceut...
By detailed study of the possible side reactions in the previously reported aziridination of alkenes...
A new process has been developed for the selective construction of 2,6-disubstituted, 2,4,6-trisubst...
A thesis describing the asymmetric syntheses of three families of amino polyols. The asymmetric synt...
Summary: Metal-catalyzed reactions have revolutionized synthetic chemistry, allowing access to unpre...
This thesis describes approaches to bicyclic nitrogen heterocycles, similar to those found in the na...
International audienceThe asymmetric synthesis of enantiopure pyrrolidines is reported via a streaml...
The synthesis of unusual cyclic amino acids, that may be envisaged as proline analogues, is an area ...
The asymmetric syntheses of 2,5-dideoxy-2,5-imino-d-glucitol [(+)-DGDP] and 1,2,5-trideoxy-1-amino-2...