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- On the Brassard's rule of regioselectivity in Diels–Alder reactions between haloquinones and polar dienes. Mauricio Maldonado-Domínguez, Karen Ruiz-Pérez, Oscar González-Antonio, Margarita Romero-Ávila, José Méndez-Stivalet, Blas Flores-Pérez
, RSC Adv.
, 2016
, 6
, 75194
- Catalytic enantioselective [4 + 2]-cycloaddition: a strategy to access aza-hexacycles. Géraldine Masson, Claudia Lalli, Meryem Benohoud, Guillaume Dagousset
, Chem. Soc. Rev.
, 2013
, 42
, 902
- Mannich–Michael versus formal aza-Diels–Alder approaches to piperidine derivatives. P. Ricardo Girling, Takao Kiyoi, Andrew Whiting
, Org. Biomol. Chem.
, 2011
, 9
, 3105
- Magnesium(ii)-catalyzed asymmetric hetero-Diels–Alder reaction of Brassard's dienes with isatins. Jianfeng Zheng, Lili Lin, Yulong Kuang, Jiannan Zhao, Xiaohua Liu, Xiaoming Feng
, Chem. Commun.
, 2014
, 50
, 994
- Enantioselective magnesium-catalyzed transformations. Hélène Pellissier
, Org. Biomol. Chem.
, 2017
, 15
, 4750
- Concise synthesis of 2,4-disubstituted thiazoles from β-azido disulfides and carboxylic acids or anhydrides: asymmetric synthesis of cystothiazole C. Yi Liu, Xue Sun, Xing Zhang, Jun Liu, Yuguo Du
, Org. Biomol. Chem.
, 2014
, 12
, 8453
- Asymmetric synthesis of (+)-teratosphaerone B, its non-natural analogue and (+)-xylarenone using an ene- and naphthol reductase cascade. Tanaya Manna, Arijit De, Khondekar Nurjamal, Syed Masood Husain
, Org. Biomol. Chem.
, 2022
, 20
, 7410
- Mechanistic studies on the formal aza-Diels–Alder reactions of N-aryl imines: evidence for the non-concertedness under Lewis-acid catalysed conditions. Stephen Hermitage, Judith A. K. Howard, David Jay, Robin G. Pritchard, Michael R. Probert, Andrew Whiting
, Org. Biomol. Chem.
, 2004
, 2
, 2451
- Catalytic enantioselective aza-Diels–Alder reactions of unactivated acyclic 1,3-dienes with aryl-, alkenyl-, and alkyl-substituted imines. Yasuo Hatanaka, Shuuto Nantaku, Yuhki Nishimura, Tomoyuki Otsuka, Tohru Sekikaw
, Chem. Commun.
, 2017
, 53
, 8996
- Synthesis and acetylation of naphthols as precursors to naturally derived naphthoquinones; crystal structure of the aphin-related 7-O-methyl quinone A. Robin G. F. Giles, Ivan R. Green, Margaret L. Niven, Selwyn C. Yorke
, J. Chem. Soc., Perkin Trans. 1
, 1988
, 2459