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- Novel hydrido-ruthenium(ii) complexes with histidine derivatives and their application in the hydrogenation of ketones. Christine Sui-Seng, Alen Hadzovic, Alan J. Lough, Robert H. Morris
, Dalton Trans.
, 2007
, 2536
- Microwave-assisted tandem allylation-isomerization reaction catalyzed by a mesostructured bifunctional catalyst in aqueous media. Guohua Liu, Yunqiang Sun, Jianyao Wang, Chuanshou Sun, Fang Zhang, Hexing Li
, Green Chem.
, 2009
, 11
, 1477
- Water-medium isomerization of homoallylic alcohol over a Ru(ii) organometallic complex immobilized on FDU-12 support. Hexing Li, Fang Zhang, Hong Yin, Ying Wan, Yunfeng Lu
, Green Chem.
, 2007
, 9
, 500
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Ruthenium-catalyzed redox isomerization/transfer hydrogenation in organic and aqueous media: A one-pot tandem process for the reduction of allylic alcohols. Victorio Cadierno, Pascale Crochet, Javier Francos, Sergio E. García-Garrido, José Gimeno, Noel Nebra
, Green Chem.
, 2009
, 11
, 1992
- Rhodium-catalysed isomerisation of allylic alcohols in water at ambient temperature. Nanna Ahlsten, Helena Lundberg, Belén Martín-Matute
, Green Chem.
, 2010
, 12
, 1628
- Oxidation of alcohols with nitroxyl radical under polymer-supported two-phase conditions. Yoshitomo Kashiwagi, Shinya Chiba, Jun-ichi Anzai
, New J. Chem.
, 2003
, 27
, 1545
- Asymmetric hydrogenation, transfer hydrogenation and hydrosilylation of ketones catalyzed by iron complexes. Robert H. Morris
, Chem. Soc. Rev.
, 2009
, 38
, 2282
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Palladium-catalyzed cross-coupling reactions of organogold(i) phosphanes with allylic electrophiles. Miguel Peña-López, Miguel Ayán-Varela, Luis A. Sarandeses, José Pérez Sestelo
, Org. Biomol. Chem.
, 2012
, 10
, 1686
- Enzymatic synthesis of enantiopure alcohols: current state and perspectives. Bi-Shuang Chen, Fayene Zeferino Ribeiro de Souza
, RSC Adv.
, 2019
, 9
, 2102
- Ionic-surfactant-coated subtilisin: activity, enantioselectivity, and application to dynamic kinetic resolution of secondary alcohols. Kyungwoo Kim, Eungyeong Lee, Cheolwoo Kim, Jaiwook Park, Mahn-Joo Kim
, Org. Biomol. Chem.
, 2017
, 15
, 8836