Development of a more efficient catalyst for the redox-neutral organocatalytic mitsunobu reaction by DFT-guided catalyst design
Tài liệu tham khảo
Emer, 2011, Eur.J. Org. Chem., 2011, 647, 10.1002/ejoc.201001474
Constable, 2007, Green Chem, 9, 411, 10.1039/B703488C
An, 2014, Org. Biomol. Chem., 12, 2993, 10.1039/c4ob00032c
Akkarasamiyo, 2018, Chem. Eur. J., 24, 3488, 10.1002/chem.201705164
Mukherjee, 2011, Org. Lett., 13, 1334, 10.1021/ol103175w
Ghebreghiorgis, 2012, J. Am. Chem. Soc., 134, 16307, 10.1021/ja306333a
Hande, 2009, J. Org. Chem., 74, 244, 10.1021/jo801926g
Mukherjee, 2013, Chem. Eur. J., 19, 3437, 10.1002/chem.201203987
Bunrit, 2015, J. Am. Chem. Soc., 137, 4646, 10.1021/jacs.5b02013
Marcyk, 2019, Angew. Chem., Int. Ed., 58, 1727, 10.1002/anie.201812894
Watile, 2019, Nat. Commun., 10, 3826, 10.1038/s41467-019-11838-x
Xiong, 2022, Green Syn. Catal., 3, 46, 10.1016/j.gresc.2021.10.005
Mitsunobu, 1967, Bull. Chem. Soc. Jpn., 40, 2380, 10.1246/bcsj.40.2380
Mitsunobu, 1981, Synthesis, 1, 1, 10.1055/s-1981-29317
Rössler, 2019, Acc. Chem. Res., 52, 2657, 10.1021/acs.accounts.9b00209
Ozawa, 2002, J. Am. Chem. Soc., 124, 10968, 10.1021/ja0274406
Bunrit, 2020, ACS Catal, 10, 1344, 10.1021/acscatal.9b03458
Nacsa, 2013, Org. Lett., 15, 38, 10.1021/ol302970c
Dryzhakov, 2016, Synthesis, 48, 935, 10.1055/s-0035-1560396
Hirose, 2016, Org. Lett., 18, 4036, 10.1021/acs.orglett.6b01894
Hirose, 2013, Angew. Chem., Int. Ed., 52, 4613, 10.1002/anie.201300153
Beddoe, 2018, Org. Biomol. Chem., 16, 7774, 10.1039/C8OB01929K
Tang, 2014, Chem. Commun., 50, 7340, 10.1039/C4CC02171A
Zhang, 2023, Asian J. Org. Chem., 12
Beddoe, 2019, Science, 365, 910, 10.1126/science.aax3353
Martin, 2022, Inorganics, 10, 35, 10.3390/inorganics10030035
Schenk, 2005, J. Am. Chem. Soc., 127, 12566, 10.1021/ja052362i
Chang, 2022, Chem, 8, 1775, 10.1016/j.chempr.2022.04.025
Zhang, 2021, J. Am. Chem. Soc., 143, 3571, 10.1021/jacs.0c13335
Zou, 2020, J. Am. Chem. Soc., 142, 16403, 10.1021/jacs.0c07487
Liu, 2023, Green Chem, 25, 3606, 10.1039/D3GC00455D
Wang, 2023, Green Chem, 25, 357, 10.1039/D2GC03679G
Yi, 2021, Org. Chem. Front., 8, 6830, 10.1039/D1QO01443A
Xiao, 2021, Chem. Commun., 57, 4690, 10.1039/D1CC00989C
Luo, 2020, Org. Chem. Front., 7, 1016, 10.1039/D0QO00140F
Ling, 2019, Org. Lett., 21, 3937, 10.1021/acs.orglett.9b01056
Ling, 2018, J. Org. Chem., 83, 10749, 10.1021/acs.joc.8b01276
Mardirossian, 2017, Mol. Phys., 115, 2315, 10.1080/00268976.2017.1333644
Wladkowski, 1995, J. Phys. Chem., 99, 4490, 10.1021/j100013a019
Matsukawa, 2002, Angew. Chem., Int. Ed., 41, 4718, 10.1002/anie.200290027
Ugi, 1971, Acc. Chem. Res., 4, 288, 10.1021/ar50044a004
Chang, 1997, J. Phys. Chem. A, 101, 8706, 10.1021/jp9718616
Moc, 1995, J. Am. Chem. Soc., 117, 11790, 10.1021/ja00152a022
Bartell, 1970, Inorg. Chem., 9, 1903, 10.1021/ic50090a021
Jiang, 2019, Chem. Sci., 10, 3466, 10.1039/C8SC05158E
Coe, 2000, Coord. Chem. Rev., 203, 5, 10.1016/S0010-8545(99)00184-8
Quagliano, 1952, Chem. Rev., 50, 201, 10.1021/cr60156a001
Neel, 2017, Nature, 543, 637, 10.1038/nature21701
Sinnokrot, 2004, J. Am. Chem. Soc., 126, 7690, 10.1021/ja049434a
Wheeler, 2008, J. Am. Chem. Soc., 130, 10854, 10.1021/ja802849j
Zhou, 2021, Green Chem, 23, 8859, 10.1039/D1GC02819G
Slavíková, 2013, J. Med. Chem., 56, 2323, 10.1021/jm3016365
