About: Diastereoselective reduction of alkenylboronic esters as a new method for controlling the stereochemistry of up to three adjacent centers in cyclic and acyclic molecules

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About: Diastereoselective reduction of alkenylboronic esters as a new method for controlling the stereochemistry of up to three adjacent centers in cyclic and acyclic molecules Goto Sponge NotDistinct Permalink

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scientific article published on 01 August 2002

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) bài báo khoa học (vi) наукова стаття, опублікована в серпні 2002 (uk) im August 2002 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu n'agostu de 2002 (ast) scientific article published on 01 August 2002 (en)
publication date	wds:Q74618891-D82FE5D2-3F84-4196-9378-9A480C8523ED
publication date	2002-08-01 00:00:00Z (xsd:dateTime)
author name string	wds:Q74618891-726749A5-76E6-496B-BA38-149F93CB7D75 wds:Q74618891-757F7954-D7FF-4271-97C6-F99A124146C9
author name string	Ilan Marek Eike Hupe
rdfs:label	Diastereoselective reduction of alkenylboronic esters as a new method for controlling the stereochemistry of up to three adjacent centers in cyclic and acyclic molecules (en) Diastereoselective reduction of alkenylboronic esters as a new method for controlling the stereochemistry of up to three adjacent centers in cyclic and acyclic molecules (nl)
skos:prefLabel	Diastereoselective reduction of alkenylboronic esters as a new method for controlling the stereochemistry of up to three adjacent centers in cyclic and acyclic molecules (en) Diastereoselective reduction of alkenylboronic esters as a new method for controlling the stereochemistry of up to three adjacent centers in cyclic and acyclic molecules (nl)
name	Diastereoselective reduction of alkenylboronic esters as a new method for controlling the stereochemistry of up to three adjacent centers in cyclic and acyclic molecules (en) Diastereoselective reduction of alkenylboronic esters as a new method for controlling the stereochemistry of up to three adjacent centers in cyclic and acyclic molecules (nl)
author	wds:Q74618891-CA225ECA-F572-472D-AEAB-BB66667BC83F
author	Paul Knochel
title	wds:Q74618891-B89352C0-C278-4379-8497-21F69A360D87
title	Diastereoselective reduction of alkenylboronic esters as a new method for controlling the stereochemistry of up to three adjacent centers in cyclic and acyclic molecules (en)
page(s)	wds:Q74618891-AB6559D7-9958-4560-BF1E-C873CF3C0362
page(s)	2861-2863
instance of	wds:Q74618891-98A87042-FCF2-4061-A473-F53BDE4AB5FF
instance of	scholarly article
PubMed ID	wds:Q74618891-308230E6-82BC-465C-B2CC-088453418D90
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/12182574
PubMed ID	12182574
published in	wds:Q74618891-95D3EA75-4D31-49E4-B55A-22DA2ED9CA21
published in	Organic Letters
issue	wds:Q74618891-A76A7A38-27D3-4C57-9E1F-2F9B2A8FB68A
volume	wds:Q74618891-798A5F9C-C66C-4568-B996-2D13B9076BD5
issue	17
volume	4
DOI	wds:Q74618891-DABDEDF8-44F9-48E5-A512-C806B9982049
DOI	http://dx.doi.org/10.1021/OL0262486
DOI	10.1021/OL0262486
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q74618891
is cites work of	Efficient C-B bond formation promoted by N-heterocyclic carbenes: synthesis of tertiary and quaternary B-substituted carbons through metal-free catalytic boron conjugate additions to cyclic and acyclic alpha,beta-unsaturated carbonyls Simple access to elusive α-boryl carbanions and their alkylation: an umpolung construction for organic synthesis. Direct stereospecific amination of alkyl and aryl pinacol boronates Catalytic Asymmetric Synthesis of Phosphine Boronates. Catalytic Asymmetric Synthesis of Phosphine Boronates Nickel-Catalyzed Stereoselective Arylboration of Unactivated Alkenes. Transition Metal-Free 1,2-Carboboration of Unactivated Alkenes. Controlled partial transfer hydrogenation of quinolines by cobalt-amido cooperative catalysis
is cites work of	wds:Q42401891-21435267-E8A0-4197-924D-225540BB7B16 wds:Q64028413-AC36BA9E-F66C-4711-BC65-E77E2D8DA66B wds:Q42563750-EEAD5263-3EB1-47B0-AE41-2076876A621A wds:Q48357236-DE05F4BB-51B6-435E-AB85-0335CAD0F708 wds:Q43179921-D8D703DB-85EE-4A69-945B-EEADC3338A76 wds:Q90117560-EFA33F33-CB1D-476F-B9E6-B756F833DF45 wds:Q52802393-A6779479-ADC4-4ABF-9B7C-482024186DF0 wds:Q55288423-EB00A7BA-562D-43A3-AB4C-3BBAE5EA6758

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