About: Organocatalytic asymmetric Mannich reactions with N-Boc and N-Cbz protected alpha-amido sulfones (Boc: tert-butoxycarbonyl, Cbz: benzyloxycarbonyl)

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About: Organocatalytic asymmetric Mannich reactions with N-Boc and N-Cbz protected alpha-amido sulfones (Boc: tert-butoxycarbonyl, Cbz: benzyloxycarbonyl) Goto Sponge Distinct Permalink

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rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована у 2007 (uk) article scientifique publié en 2007 (fr) im Januar 2007 veröffentlichter wissenschaftlicher Artikel (de)
publication date	wds:Q56996209-55BFE5D1-ADE8-4588-BE19-4850BF0D3E8C wds:Q56996209-59E4E973-8C06-49A0-9B1D-DEFAC8366565
publication date	2007-01-01 00:00:00Z (xsd:dateTime) 2007-10-05 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q56996209-B6A8550A-E6F4-455C-B34E-7AAD7113F15D
language of work or name	English
author name string	wds:Q56996209-5368AB3A-EAEA-4300-BCF1-CFE74106FBE4 wds:Q56996209-71982E62-F018-46AA-8A40-393FC0A0310C wds:Q56996209-76332D8B-AB7D-49B9-85AC-93F7C7278335 wds:Q56996209-EF40DE4D-4F29-4D7E-8A39-D8C43E7AE7A3 wds:Q56996209-F36654EA-2EB7-4FCD-ABE1-F58F569A00B4
author name string	Alfredo Ricci Daniel Pettersen Gabriele Micheletti Valentina Sgarzani Olindo Marianacci
rdfs:label	Organocatalytic asymmetric Mannich reactions with N-Boc and N-Cbz protected alpha-amido sulfones (Boc: tert-butoxycarbonyl, Cbz: benzyloxycarbonyl) (en) Organocatalytic asymmetric Mannich reactions with N-Boc and N-Cbz protected alpha-amido sulfones (Boc: tert-butoxycarbonyl, Cbz: benzyloxycarbonyl) (nl)
skos:prefLabel	Organocatalytic asymmetric Mannich reactions with N-Boc and N-Cbz protected alpha-amido sulfones (Boc: tert-butoxycarbonyl, Cbz: benzyloxycarbonyl) (en) Organocatalytic asymmetric Mannich reactions with N-Boc and N-Cbz protected alpha-amido sulfones (Boc: tert-butoxycarbonyl, Cbz: benzyloxycarbonyl) (nl)
name	Organocatalytic asymmetric Mannich reactions with N-Boc and N-Cbz protected alpha-amido sulfones (Boc: tert-butoxycarbonyl, Cbz: benzyloxycarbonyl) (en) Organocatalytic asymmetric Mannich reactions with N-Boc and N-Cbz protected alpha-amido sulfones (Boc: tert-butoxycarbonyl, Cbz: benzyloxycarbonyl) (nl)
author	wds:Q56996209-119F6289-7F84-489B-991A-DE30C653C2B3 wds:Q56996209-358D1671-DBCD-44AB-954F-E560BB54ABE0 wds:Q56996209-A0782798-65FB-4ADC-A491-AB5F1E222F60
author	Luca Bernardi Mariafrancesca Fochi Francesco Fini
title	wds:Q56996209-0B018C5E-56D4-4D9D-A1BC-541D70980D88 wds:Q56996209-9F014D88-9FA2-4AAC-85CA-B1B400471A7B
title	Organocatalytic Asymmetric Mannich Reactions withN-Boc andN-Cbz Protected α-Amido Sulfones (Boc:tert-Butoxycarbonyl, Cbz: Benzyloxycarbonyl) (en) Organocatalytic asymmetric Mannich reactions with N-Boc and N-Cbz protected alpha-amido sulfones (Boc: tert-butoxycarbonyl, Cbz: benzyloxycarbonyl) (en)
page(s)	wds:Q56996209-0177F5E4-31DF-4824-BAF2-85B808FBC8B5 wds:Q56996209-70BD1FD0-1835-4F82-A547-89816A2FF895
page(s)	8338-8351 8338-51
instance of	wds:Q56996209-A801F0A3-343F-4C07-8AA4-A354DBD7CC68
instance of	scholarly article
main subject	wds:Q56996209-2AEAB6CF-D6F4-4688-BA48-9EFC3157E6EC wds:Q56996209-DF5703F4-A3A5-45DB-992B-5628304208BD
main subject	general chemistry Organocatalysis
PubMed ID	wds:Q56996209-9ACEB55D-8CF1-4D74-A9C1-59789ED92A4F
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/17705329
PubMed ID	17705329
published in	wds:Q56996209-7443C9FB-8381-4AE7-B42D-4533A1EDA69E
published in	Chemistry—A European Journal
issue	wds:Q56996209-587EA64C-9549-454A-A474-86F4131F22EF
volume	wds:Q56996209-0AF3B4B7-F0CE-42F5-86FB-0BC89B7287A2
issue	29
volume	13
DOI	wds:Q56996209-A1BC56EA-F88D-44FC-A203-CBA2FC3AC5C1
DOI	http://dx.doi.org/10.1002/CHEM.200700908
DOI	10.1002/CHEM.200700908
skos:altLabel	Organocatalytic Asymmetric Mannich Reactions withN-Boc andN-Cbz Protected α-Amido Sulfones (Boc:tert-Butoxycarbonyl, Cbz: Benzyloxycarbonyl) (en) Organocatalytic Asymmetric Mannich Reactions withN-Boc andN-Cbz Protected α-Amido Sulfones (Boc:tert-Butoxycarbonyl, Cbz: Benzyloxycarbonyl) (nl)
is owl:sameAs of	Organocatalytic asymmetric Mannich reactions with N-Boc and N-Cbz protected alpha-amido sulfones (Boc: tert-butoxycarbonyl, Cbz: benzyloxycarbonyl)
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q56996209
is cites work of	Organocatalytic, diastereo- and enantioselective synthesis of nonsymmetric cis-stilbene diamines: a platform for the preparation of single-enantiomer cis-imidazolines for protein-protein inhibition Catalytic, Enantioselective Synthesis of Stilbene cis-Diamines: A Concise Preparation of (-)-Nutlin-3, a Potent p53/MDM2 Inhibitor Organocatalytic, enantioselective synthesis of VNI: a robust therapeutic development platform for Chagas, a neglected tropical disease Recent developments in asymmetric phase-transfer reactions Highly efficient catalytic enantioselective Mannich reaction of malonates with N-tert-butoxycarbonyl imines by using Yb(OTf)3/pybox catalysts at room temperature Three-component Ag-catalyzed enantioselective vinylogous mannich and Aza-Diels-Alder reactions with alkyl-substituted aldehydes Enantioselective synthesis of benzoindolizidine derivatives using chiral phase-transfer catalytic intramolecular domino aza-Michael addition/alkylation. Brønsted acid catalyzed Morita-Baylis-Hillman reaction: a new mechanistic view for thioureas revealed by ESI-MS(/MS) monitoring and DFT calculations. Organocatalytic asymmetric synthesis of propargylamines with two adjacent stereocenters: mannich-type reactions of in situ generated C-alkynyl imines with β-keto esters. A carbon nanotube confinement strategy to implement homogeneous asymmetric catalysis in the solid phase. The homo-PADAM protocol: stereoselective and operationally simple synthesis of α-oxo- or α-hydroxy-γ-acylaminoamides and chromanes. Asymmetric Protonation of Cumulenolates: Synthesis of Allenyl Aldehydes Facilitated by an Organomanganese Auxiliary Organocatalytic asymmetric synthesis of β(3)-amino acid derivatives A novel homobimetallic nickel complex for the asymmetric direct Mannich reaction of imines: a practical method on a multi-gram scale Dynamic Covalent Chemistry of Nucleophilic Substitution Component Exchange of Quaternary Ammonium Salts 1-Imidoalkylphosphonium salts with modulated Cα-P+ bond strength: synthesis and application as new active α-imidoalkylating agents. 1-(-Acylamino)alkyltriarylphosphonium Salts with Weakened C-P⁺ Bond Strength-Synthetic Applications The Synthesis of α-Aminophosphonates via Enantioselective Organocatalytic Reaction of 1-(N-Acylamino)alkylphosphonium Salts with Dimethyl Phosphite
is cites work of	wds:Q33998827-C98CD55B-5170-46D4-923F-E9C7BC7271D6 wds:Q45356522-0D69F185-24AC-48B1-B5B3-83BD7EBDF547 wds:Q51032405-8A95715A-3649-4231-A693-406D752C3CA7 wds:Q51012624-17B81A5C-2E5E-4D04-AC24-140D86D7863E wds:Q51831564-8A7F5F6E-11F2-485F-9205-B31EE873856F wds:Q46452484-8BE82D82-FB40-479F-8DAA-BAD7892DF125 wds:Q46259870-A2EE694E-766B-4E3F-A8B6-5ED505CC099E wds:Q45202880-FC9D1B84-D8A7-4C64-BB05-4421E7CCC9D5 wds:Q24597322-EE2F1A0F-3B32-404E-8B71-14EFF6BD4BEF wds:Q43265233-702A9FD5-492E-4611-9473-55A0C18D6E54 wds:Q35715069-13BADA54-885D-4779-94B2-FF976F1D7D2A wds:Q46141038-B4C59B7E-A558-4766-82B9-F4F54CD90A1C wds:Q37149448-0CC2E725-4092-499C-986D-F03B3ABFB35B wds:Q42202669-D49A6DED-BD63-432D-8F2E-FF5DC6539CA1 wds:Q58692243-8FEA8864-55B3-468B-B176-43ACAFBEDCDD wds:Q41334941-DE802457-A6F7-4E05-B9C8-47365DF3EA7B wds:Q42380730-039E7A6F-775D-4194-B814-9FF9DB703568 wds:Q92813986-8652EE81-6086-426A-85D0-A62440959109

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