Index
A
Acrylate, 6, 17, 18
Alcohol, 7, 45, 50, 62, 64, 150, 152, 187,
189, 192, 218, 219, 228, 244, 248,
266, 269, 307, 308, 334
Aldehyde, 3, 7, 8, 12, 14, 178, 220, 221, 244,
248, 260, 261, 272, 327, 333, 334
Alkene, 6, 13, 14, 17, 31, 35, 38, 125, 126,
128, 140, 150, 152, 156, 173, 226,
240, 248, 249, 257, 266–268, 272,
326, 327, 337, 338, 362
Alkyne, 6, 7, 14–17, 31, 90, 135, 137–139,
141, 150, 152, 156, 226, 240, 242,
248, 249, 266, 267, 272, 326, 334,
336, 344, 362
Amination, 1, 15, 79, 221–224
Amine, 8, 10, 31, 33, 73, 75, 80, 120, 122,
147, 148, 150, 151, 174, 179, 185,
188, 221, 227, 240, 243, 248, 253,
259, 287, 303, 310, 325–327, 329,
331, 335, 363, 379
Asymmetric catalysis, 29, 31, 47, 69, 259,
273
Asymmetric hydrogenation, 11, 31–41, 43,
45, 47, 50, 51, 55, 56, 58–62, 226,
240
Asymmetric hydrosilylation, 57, 59, 63, 65,
67, 69, 70
Asymmetric transfer hydrogenation, 13, 69,
73–78
B
Bimetallic compounds, 342, 346
Biomass, 297, 299, 312
Borane, 2–4, 6–8, 12–15, 31, 32, 35, 38, 40,
43, 45, 57, 59, 62, 64, 67, 69, 73, 75,
89, 90, 92–94, 96–99, 101, 102, 104,
120, 123, 124, 134, 140, 144, 150,
156, 171, 174, 176, 177, 180, 184–
186, 190, 193, 209, 211–229, 240,
242, 287, 320, 322, 325, 326, 330,
333, 334, 362, 380
Borylation, 1, 16, 17, 117, 119–131, 133,
134, 139–148, 150–157, 250, 251,
330, 344, 345
C
Carbene, 2, 17, 35, 88, 96, 169, 284, 285,
335
Carbon dioxide, 97, 101, 248, 325
Carbon monoxide, 87–90, 92, 94, 96–102,
104, 105, 331, 333
C–F derivatization, 1, 18
C–H activation, 115–118, 120, 125, 126,
135, 136, 138–142, 145–152, 158,
160, 250, 263
Charge-transfer complex, 378
Chiral, 13, 29, 31–33, 35, 38–40, 42, 43, 45,
47, 54, 57, 59, 61–64, 67–69, 75, 78,
81, 98, 226–229, 239, 240, 259, 273,
303, 304, 331
Classical Lewis Adduct (CLA), 210, 283,
284, 362, 396
Cooperative chemistry, 320
Curriculum, 387–389, 391, 397
Cyclic ester, 283, 286–288, 302, 307, 308,
312
D
Density functional theory (DFT), 35, 95,
124, 136, 142, 145, 146, 150, 154,
© Springer Nature Switzerland AG 2021
J. Chris Slootweg and A. R. Jupp (eds.), Frustrated Lewis Pairs,
Molecular Catalysis 2, https://doi.org/10.1007/978-3-030-58888-5
401
A
Acrylate, 6, 17, 18
Alcohol, 7, 45, 50, 62, 64, 150, 152, 187,
189, 192, 218, 219, 228, 244, 248,
266, 269, 307, 308, 334
Aldehyde, 3, 7, 8, 12, 14, 178, 220, 221, 244,
248, 260, 261, 272, 327, 333, 334
Alkene, 6, 13, 14, 17, 31, 35, 38, 125, 126,
128, 140, 150, 152, 156, 173, 226,
240, 248, 249, 257, 266–268, 272,
326, 327, 337, 338, 362
Alkyne, 6, 7, 14–17, 31, 90, 135, 137–139,
141, 150, 152, 156, 226, 240, 242,
248, 249, 266, 267, 272, 326, 334,
336, 344, 362
Amination, 1, 15, 79, 221–224
Amine, 8, 10, 31, 33, 73, 75, 80, 120, 122,
147, 148, 150, 151, 174, 179, 185,
188, 221, 227, 240, 243, 248, 253,
259, 287, 303, 310, 325–327, 329,
331, 335, 363, 379
Asymmetric catalysis, 29, 31, 47, 69, 259,
273
Asymmetric hydrogenation, 11, 31–41, 43,
45, 47, 50, 51, 55, 56, 58–62, 226,
240
Asymmetric hydrosilylation, 57, 59, 63, 65,
67, 69, 70
Asymmetric transfer hydrogenation, 13, 69,
73–78
B
Bimetallic compounds, 342, 346
Biomass, 297, 299, 312
Borane, 2–4, 6–8, 12–15, 31, 32, 35, 38, 40,
43, 45, 57, 59, 62, 64, 67, 69, 73, 75,
89, 90, 92–94, 96–99, 101, 102, 104,
120, 123, 124, 134, 140, 144, 150,
156, 171, 174, 176, 177, 180, 184–
186, 190, 193, 209, 211–229, 240,
242, 287, 320, 322, 325, 326, 330,
333, 334, 362, 380
Borylation, 1, 16, 17, 117, 119–131, 133,
134, 139–148, 150–157, 250, 251,
330, 344, 345
C
Carbene, 2, 17, 35, 88, 96, 169, 284, 285,
335
Carbon dioxide, 97, 101, 248, 325
Carbon monoxide, 87–90, 92, 94, 96–102,
104, 105, 331, 333
C–F derivatization, 1, 18
C–H activation, 115–118, 120, 125, 126,
135, 136, 138–142, 145–152, 158,
160, 250, 263
Charge-transfer complex, 378
Chiral, 13, 29, 31–33, 35, 38–40, 42, 43, 45,
47, 54, 57, 59, 61–64, 67–69, 75, 78,
81, 98, 226–229, 239, 240, 259, 273,
303, 304, 331
Classical Lewis Adduct (CLA), 210, 283,
284, 362, 396
Cooperative chemistry, 320
Curriculum, 387–389, 391, 397
Cyclic ester, 283, 286–288, 302, 307, 308,
312
D
Density functional theory (DFT), 35, 95,
124, 136, 142, 145, 146, 150, 154,
© Springer Nature Switzerland AG 2021
J. Chris Slootweg and A. R. Jupp (eds.), Frustrated Lewis Pairs,
Molecular Catalysis 2, https://doi.org/10.1007/978-3-030-58888-5
401