(PDF) Stereoselective Synthesis of 1,2-Amino Alcohols by

Stereoselective Synthesis of 1,2-Amino Alcohols by Addition of Organocuprate·BF3 Complexes and Organolithium Reagents to an Α-Silyloxyaldimine Derived From (S)-Ethyl Lactate

Tetrahedron - United Kingdom

doi 10.1016/0040-4020(96)00776-4

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October 1, 1996

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Elsevier BV

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Stereoselective Synthesis of 1,2-Amino Alcohols by Addition of Organocuprate·BF3 Complexes and Organolithium Reagents to an Α-Silyloxyaldimine Derived From (S)-Ethyl Lactate

Tetrahedron - United Kingdom

doi 10.1016/0040-4020(96)00776-4

Full Text

Abstract

Categories

Date

Authors

Publisher

Related search

Synthesis of 3–aryl 3–hydroxyisoindolinones by the Addition of Grignard and Organolithium Reagents to Phthalimides

Synthesis of Enantiopure (aS, bS)- Or (aR, bS)-b-Amino Alcohols by Complete Regioselective Opening of Aminoepoxides by Organolithium Reagents LiAlH4 or LiAlD4

STEREOSELECTIVE FORMATION OF Α,α-Diamino ACID RESIDUE BY THE ADDITION OF L-Α-Amino ACID TO Α-Imino ACID

Organolithium-Induced Alkylative Ring Opening of Aziridines: Synthesis of Unsaturated Amino Alcohols and Ethers

A Convenient Reduction of Α-Amino Acids to 1,2-Amino Alcohols With Retention of Optical Purity

2Azadienes as Reagents for Preparing Chiral Amines: Synthesis of 1,2-Amino Tertiary Alcohols by Cu-Catalyzed Enantioselective Reductive Couplings With Ketones

2Azadienes as Reagents for Preparing Chiral Amines: Synthesis of 1,2-Amino Tertiary Alcohols by Cu-Catalyzed Enantioselective Reductive Couplings With Ketones

Synthesis of Α,ω-Bis-Enones by the Double Addition of Alkenyl Grignard Reagents to Diacid Weinreb Amides

Enantioselective Addition of Allyltin Reagents to Amino Aldehydes Catalyzed With Bis(oxazolinyl)phenylrhodium(III) Aqua Complexes