Diisopinocampheylborane-mediated reductive aldol reactions: highly enantio- and diastereoselective synthesis of syn aldols from N-acryloylmorpholine.
about
Synthesis of (+)-discodermolide by catalytic stereoselective borylation reactions.(Diisopinocampheyl)borane-mediated reductive aldol reactions of acrylate esters: enantioselective synthesis of anti-aldolsEnantio- and diastereoselective synthesis of syn-β-hydroxy-α-vinyl carboxylic esters via reductive aldol reactions of ethyl allenecarboxylate with 10-TMS-9-Borabicyclo[3.3.2]decane and DFT analysis of the hydroboration pathway.Generation of stereochemically defined tetrasubstituted enolborinates by 1,4-hydroboration of α,β-unsaturated morpholine carboxamides with (diisopinocampheyl)borane.
P2860
Diisopinocampheylborane-mediated reductive aldol reactions: highly enantio- and diastereoselective synthesis of syn aldols from N-acryloylmorpholine.
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article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on July 2013
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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Diisopinocampheylborane-mediat ...... ols from N-acryloylmorpholine.
@en
Diisopinocampheylborane-mediat ...... ols from N-acryloylmorpholine.
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type
label
Diisopinocampheylborane-mediat ...... ols from N-acryloylmorpholine.
@en
Diisopinocampheylborane-mediat ...... ols from N-acryloylmorpholine.
@nl
prefLabel
Diisopinocampheylborane-mediat ...... ols from N-acryloylmorpholine.
@en
Diisopinocampheylborane-mediat ...... ols from N-acryloylmorpholine.
@nl
P2093
P2860
P356
P1476
Diisopinocampheylborane-mediat ...... ols from N-acryloylmorpholine.
@en
P2093
Christophe Allais
Philippe Nuhant
William R Roush
P2860
P304
P356
10.1002/ANIE.201302535
P407
P577
2013-07-01T00:00:00Z