Corrigendum to “Aldol reaction via in situ olefin migration in water”

2002 ◽  
Vol 43 (31) ◽  
pp. 5503
Author(s):  
Mingwen Wang ◽  
Chao-Jun Li
Keyword(s):  
Aldol Reaction ◽  
Olefin Migration

Aldol reaction via in situ olefin migration in water

2002 ◽  
Vol 43 (19) ◽  
pp. 3589-3591 ◽  
Author(s):  
Mingwen Wang ◽  
Chao-Jun Li
Keyword(s):  
Aldol Reaction ◽  
Olefin Migration

ChemInform Abstract: Aldol Reaction via in situ Olefin Migration in Water.

ChemInform ◽  
2010 ◽  
Vol 33 (34) ◽  
pp. no-no
Author(s):  
Mingwen Wang ◽  
Chao-Jun Li
Keyword(s):  
Aldol Reaction ◽  
Olefin Migration

ChemInform Abstract: Rhodium-Catalyzed Cross-Aldol Reaction: In situ Aldehyde-Enolate Formation from Allyloxyboranes and Primary Allylic Alcohols.

ChemInform ◽  
2013 ◽  
Vol 44 (11) ◽  
pp. no-no
Author(s):  
Luqing Lin ◽  
Kumiko Yamamoto ◽  
Shigeki Matsunaga ◽  
Motomu Kanai
Keyword(s):  
Aldol Reaction ◽  
Allylic Alcohols

Rh-Catalyzed AldehydeAldehyde Cross-Aldol Reaction under Base-Free Conditions: In Situ Aldehyde-Derived Enolate Formation through Orthogonal Activation

2013 ◽  
Vol 8 (12) ◽  
pp. 2974-2983 ◽  
Author(s):  
Luqing Lin ◽  
Kumiko Yamamoto ◽  
Shigeki Matsunaga ◽  
Motomu Kanai
Keyword(s):  
Aldol Reaction

A Catalytic Aldol Reaction and Condensation through In Situ Boron “Ate” Complex Enolate Generation in Water

2008 ◽  
Vol 47 (4) ◽  
pp. 768-770 ◽  
Author(s):  
Karel Aelvoet ◽  
Andrei S. Batsanov ◽  
Alexandrea J. Blatch ◽  
Christophe Grosjean ◽  
Leonard G. F. Patrick ◽  
...  
Keyword(s):  
Aldol Reaction

Chiral Silver Alkoxide Catalyzed Asymmetric Aldol Reaction of Alkenyl Esters with Isatins

Synlett ◽  
2021 ◽  
Author(s):  
Akira Yanagisawa ◽  
Aiko Kawada
Keyword(s):  
Aldol Reaction ◽  
Optically Active ◽  
Asymmetric Aldol ◽  
Asymmetric Aldol Reaction ◽  
High Yields

AbstractA catalytic enantioselective aldol reaction of alkenyl esters with isatins was achieved using a DM-BINAP·AgOTf complex as the chiral precatalyst and N,N-diisopropylethylamine as the base precatalyst in the presence of methanol or 2,2,2-trifluoroethanol. Optically active 3-alkylated 3-hydroxy-2-oxindoles having up to 98% ee were diastereoselectively obtained in moderate to high yields not only from cyclic alkenyl esters but also from acyclic ones through the in situ generated chiral silver enolates.

Temperature-controlled Mukaiyama aldol reaction of cyclododecanone (CDD) with aromatic aldehydes promoted by TMSCl via the (TMS)3Si intermediate generated in situ

2016 ◽  
Vol 40 (4) ◽  
pp. 3833-3842 ◽  
Author(s):  
Venkatesan Sathesh ◽  
Kulathu I. Sathiyanarayanan
Keyword(s):  
Aldol Reaction ◽  
Aromatic Aldehydes ◽  
Diastereoselective Synthesis ◽  
Mukaiyama Aldol Reaction ◽  
Mukaiyama Aldol ◽  
Temperature Controlled ◽  
Sterically Hindered

A temperature controlled chemo-, regio- and diastereoselective synthesis of enones and Mukaiyama aldol reaction have been developed using sterically hindered CDD with organosilane as a catalyst.

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