This protocol describes a procedure for the synthesis of α, β-branched-b-amino aldehydes via Proline-catalyzed asymmetric Mannich reaction of aldehydes with N-tert–butoxycarbonyl-imines. The crystalline β-amino aldehydes are formed in good yields and extremely high levels of diastereo- and enantioselectivities without the need for chromatographic purification and are readily oxidized to the corresponding β-amino acids. The protocol can be completed in approximately 14 h on small scales or up to 30 h on larger scales
Here we report a new catalytic asymmetric synthesis of oxazolidin-2-ones 4 and Cbz-protected 1,2-ami...
A catalytic diastereoselective Mannich reaction promoted by chiral bifunctional urea-type organocata...
Enantiomerically pure 3-methyl-β-proline was synthesized using an asymmetric phase-transfer-catalyze...
We have developed proline-catalyzed direct asymmetric three-component Mannich reactions of ketones, ...
Small organic molecules recently emerged as a third class of broadly useful asymmetric catalysts tha...
Mannich reaction occuring among ketone, aldehyde, and amine is one of the ways of a synthesis of bio...
The first direct catalytic asymmetric α-amination of aldehydes is described herein. α-Unbranched ald...
Double‐cross: Proline catalyzes the double Mannich reaction of acetaldehyde with N‐Boc imines in exc...
Mannich-type reactions are powerful methods for the efficient synthesis of beta-amino carbonyl compo...
Mannich-type reactions are powerful methods for the efficient synthesis of beta-amino carbonyl compo...
A highly enantioselective catalytic route to carbamate- and benzoate-protected β-amino aldehydes and...
In recent years, L-proline has been employed as the catalyst for the intra-and intermolecular aldol ...
Abstract—The first direct organocatalytic asymmetric Mannich-type reactions in aqueous media are dem...
This account focuses on novel amine-catalyzed reactions recently discovered in our laboratories. Amo...
Here we report a new catalytic asymmetric synthesis of oxazolidin-2-ones 4 and Cbz-protected 1,2-ami...
Here we report a new catalytic asymmetric synthesis of oxazolidin-2-ones 4 and Cbz-protected 1,2-ami...
A catalytic diastereoselective Mannich reaction promoted by chiral bifunctional urea-type organocata...
Enantiomerically pure 3-methyl-β-proline was synthesized using an asymmetric phase-transfer-catalyze...
We have developed proline-catalyzed direct asymmetric three-component Mannich reactions of ketones, ...
Small organic molecules recently emerged as a third class of broadly useful asymmetric catalysts tha...
Mannich reaction occuring among ketone, aldehyde, and amine is one of the ways of a synthesis of bio...
The first direct catalytic asymmetric α-amination of aldehydes is described herein. α-Unbranched ald...
Double‐cross: Proline catalyzes the double Mannich reaction of acetaldehyde with N‐Boc imines in exc...
Mannich-type reactions are powerful methods for the efficient synthesis of beta-amino carbonyl compo...
Mannich-type reactions are powerful methods for the efficient synthesis of beta-amino carbonyl compo...
A highly enantioselective catalytic route to carbamate- and benzoate-protected β-amino aldehydes and...
In recent years, L-proline has been employed as the catalyst for the intra-and intermolecular aldol ...
Abstract—The first direct organocatalytic asymmetric Mannich-type reactions in aqueous media are dem...
This account focuses on novel amine-catalyzed reactions recently discovered in our laboratories. Amo...
Here we report a new catalytic asymmetric synthesis of oxazolidin-2-ones 4 and Cbz-protected 1,2-ami...
Here we report a new catalytic asymmetric synthesis of oxazolidin-2-ones 4 and Cbz-protected 1,2-ami...
A catalytic diastereoselective Mannich reaction promoted by chiral bifunctional urea-type organocata...
Enantiomerically pure 3-methyl-β-proline was synthesized using an asymmetric phase-transfer-catalyze...