-
1
-
-
0000369244
-
-
W. Oppolzer, R. Moretti, G. Bernardinelli, Tetrahedron Lett. 1986, 27, 4713–4716;
-
(1986)
Tetrahedron Lett.
, vol.27
, pp. 4713-4716
-
-
Oppolzer, W.1
Moretti, R.2
Bernardinelli, G.3
-
2
-
-
0242659004
-
-
S. Hanessian, Y. Yang, S. Giroux, V. Mascitti, J. Ma, F. Raeppel, J. Am. Chem. Soc. 2003, 125, 13784–13792;
-
(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 13784-13792
-
-
Hanessian, S.1
Yang, Y.2
Giroux, S.3
Mascitti, V.4
Ma, J.5
Raeppel, F.6
-
4
-
-
22744455753
-
-
Angew. Chem. 2004, 116, 3878–3880;
-
(2004)
Angew. Chem.
, vol.116
, pp. 3878-3880
-
-
-
5
-
-
1942533588
-
-
E. Negishi, Z. Tan, B. Liang, T. Novak, Proc. Natl. Acad. Sci. USA 2004, 101, 5782–5787;
-
(2004)
Proc. Natl. Acad. Sci. USA
, vol.101
, pp. 5782-5787
-
-
Negishi, E.1
Tan, Z.2
Liang, B.3
Novak, T.4
-
6
-
-
22244475838
-
-
R. D. Mazery, M. Pullez, F. Lopez, S. R. Harutyunyan, A. J. Minnaard, B. L. Feringa, J. Am. Chem. Soc. 2005, 127, 9966–9967;
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 9966-9967
-
-
Mazery, R.D.1
Pullez, M.2
Lopez, F.3
Harutyunyan, S.R.4
Minnaard, A.J.5
Feringa, B.L.6
-
7
-
-
34547929795
-
-
B. ter Horst, B. L. Feringa, A. J. Minnard, Org. Lett. 2007, 9, 3013–3015;
-
(2007)
Org. Lett.
, vol.9
, pp. 3013-3015
-
-
ter Horst, B.1
Feringa, B.L.2
Minnard, A.J.3
-
9
-
-
34548325341
-
-
Angew. Chem. 2007, 119, 1147–1149;
-
(2007)
Angew. Chem.
, vol.119
, pp. 1147-1149
-
-
-
10
-
-
70349907595
-
-
G. J. Brand, C. Studte, B. Breit, Org. Lett. 2009, 11, 4668–4670;
-
(2009)
Org. Lett.
, vol.11
, pp. 4668-4670
-
-
Brand, G.J.1
Studte, C.2
Breit, B.3
-
11
-
-
78149250621
-
-
for selected reviews, see
-
S. B. Han, A. Hassan, I. S. Kim, M. J. Krische, J. Am. Chem. Soc. 2010, 132, 15559–15561; for selected reviews, see:
-
(2010)
J. Am. Chem. Soc.
, vol.132
, pp. 15559-15561
-
-
Han, S.B.1
Hassan, A.2
Kim, I.S.3
Krische, M.J.4
-
14
-
-
77950487924
-
-
Angew. Chem. 2009, 121, 5342–5346;
-
(2009)
Angew. Chem.
, vol.121
, pp. 5342-5346
-
-
-
15
-
-
77950343374
-
-
B. ter Horst, B. L. Feringa, A. J. Minnard, Chem. Commun. 2010, 46, 2535–2547.
-
(2010)
Chem. Commun.
, vol.46
, pp. 2535-2547
-
-
ter Horst, B.1
Feringa, B.L.2
Minnard, A.J.3
-
16
-
-
14844330075
-
-
T. Novak, Z. Tan, B. Liang, E. Negishi, J. Am. Chem. Soc. 2005, 127, 2838–2839;
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 2838-2839
-
-
Novak, T.1
Tan, Z.2
Liang, B.3
Negishi, E.4
-
17
-
-
40149088849
-
-
J. Lee, K. C. Gray, J. S. Paek, M. D. Burke, J. Am. Chem. Soc. 2008, 130, 466–468;
-
(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 466-468
-
-
Lee, J.1
Gray, K.C.2
Paek, J.S.3
Burke, M.D.4
-
18
-
-
84901381097
-
-
E. M. Woerly, J. Roy, M. D. Burke, Nat. Chem. 2014, 6, 484–491.
-
(2014)
Nat. Chem.
, vol.6
, pp. 484-491
-
-
Woerly, E.M.1
Roy, J.2
Burke, M.D.3
-
20
-
-
77957201532
-
-
Angew. Chem. 2010, 122, 2807–2809;
-
(2010)
Angew. Chem.
, vol.122
, pp. 2807-2809
-
-
-
22
-
-
84950257445
-
-
L. Lin, K. Yamamoto, H. Mitsunuma, Y. Kanzaki, S. Matsunaga, M. Kanai, J. Am. Chem. Soc. 2015, 137, 15418–15421.
-
(2015)
J. Am. Chem. Soc.
, vol.137
, pp. 15418-15421
-
-
Lin, L.1
Yamamoto, K.2
Mitsunuma, H.3
Kanzaki, Y.4
Matsunaga, S.5
Kanai, M.6
-
23
-
-
84907279720
-
-
M. Burns, S. Essafi, J. R. Bame, S. P. Bull, M. P. Webster, S. Balieu, J. W. Dale, C. P. Butts, J. N. Harvey, V. K. Aggarwal, Nature 2014, 513, 183–188.
-
(2014)
Nature
, vol.513
, pp. 183-188
-
-
Burns, M.1
Essafi, S.2
Bame, J.R.3
Bull, S.P.4
Webster, M.P.5
Balieu, S.6
Dale, J.W.7
Butts, C.P.8
Harvey, J.N.9
Aggarwal, V.K.10
-
24
-
-
85043931843
-
-
For iterative boronic ester homologation with α-chloroalkyllithium reagents, see
-
For iterative boronic ester homologation with α-chloroalkyllithium reagents, see:
-
-
-
-
27
-
-
84926433821
-
-
S. Balieu, G. E. Hallett, M. Burns, T. Bootwicha, J. Studley, V. K. Aggarwal, J. Am. Chem. Soc. 2015, 137, 4398–4403;
-
(2015)
J. Am. Chem. Soc.
, vol.137
, pp. 4398-4403
-
-
Balieu, S.1
Hallett, G.E.2
Burns, M.3
Bootwicha, T.4
Studley, J.5
Aggarwal, V.K.6
-
28
-
-
70349925853
-
-
G. Dutheuil, M. P. Webster, P. A. Worthington, V. K. Aggarwal, Angew. Chem. Int. Ed. 2009, 48, 6317–6319;
-
(2009)
Angew. Chem. Int. Ed.
, vol.48
, pp. 6317-6319
-
-
Dutheuil, G.1
Webster, M.P.2
Worthington, P.A.3
Aggarwal, V.K.4
-
29
-
-
77950836318
-
-
Angew. Chem. 2009, 121, 6435–6437.
-
(2009)
Angew. Chem.
, vol.121
, pp. 6435-6437
-
-
-
30
-
-
79953230471
-
-
G. Ni, Z.-F. Shen, Y. Lu, Y.-H. Wang, Y.-B. Tang, R.-Y. Chen, Z.-Y. Hao, D.-Q. Yu, J. Org. Chem. 2011, 76, 2056–2061.
-
(2011)
J. Org. Chem.
, vol.76
, pp. 2056-2061
-
-
Ni, G.1
Shen, Z.-F.2
Lu, Y.3
Wang, Y.-H.4
Tang, Y.-B.5
Chen, R.-Y.6
Hao, Z.-Y.7
Yu, D.-Q.8
-
31
-
-
0032709549
-
-
D. H. S. Silva, S. C. Davino, S. B. de Moraes Barros, M. Yoshida, J. Nat. Prod. 1999, 62, 1475–1478.
-
(1999)
J. Nat. Prod.
, vol.62
, pp. 1475-1478
-
-
Silva, D.H.S.1
Davino, S.C.2
de Moraes Barros, S.B.3
Yoshida, M.4
-
32
-
-
84876840315
-
-
Q. Xiao, J. J. Jackson, A. Basak, J. M. Bowler, B. G. Miller, A. Zakarian, Nat. Chem. 2013, 5, 410–416.
-
(2013)
Nat. Chem.
, vol.5
, pp. 410-416
-
-
Xiao, Q.1
Jackson, J.J.2
Basak, A.3
Bowler, J.M.4
Miller, B.G.5
Zakarian, A.6
-
33
-
-
85043843538
-
-
For the generation of enantioenriched lithiated primary alkyl benzoates, see
-
For the generation of enantioenriched lithiated primary alkyl benzoates, see:
-
-
-
-
34
-
-
80055005815
-
-
R. Larouche-Gauthier, C. J. Fletcher, I. Couto, V. K. Aggarwal, Chem. Commun. 2011, 47, 12592–12594;
-
(2011)
Chem. Commun.
, vol.47
, pp. 12592-12594
-
-
Larouche-Gauthier, R.1
Fletcher, C.J.2
Couto, I.3
Aggarwal, V.K.4
-
36
-
-
85043961261
-
-
see references [4] and [6a].
-
see references [4] and [6a].
-
-
-
-
37
-
-
85043922653
-
-
For the generation of enantioenriched lithiated primary alkyl carbamates, see
-
For the generation of enantioenriched lithiated primary alkyl carbamates, see:
-
-
-
-
38
-
-
0343583098
-
-
D. Hoppe, F. Hintze, P. Tebben, Angew. Chem. Int. Ed. Engl. 1990, 29, 1422–1424;
-
(1990)
Angew. Chem. Int. Ed. Engl.
, vol.29
, pp. 1422-1424
-
-
Hoppe, D.1
Hintze, F.2
Tebben, P.3
-
39
-
-
0001488536
-
-
for a review, see
-
Angew. Chem. 1990, 102, 1457–1459; for a review, see:
-
(1990)
Angew. Chem.
, vol.102
, pp. 1457-1459
-
-
-
41
-
-
0000854142
-
-
for selected examples of application in lithiation–borylations, see
-
Angew. Chem. 1997, 109, 2376–2410; for selected examples of application in lithiation–borylations, see:
-
(1997)
Angew. Chem.
, vol.109
, pp. 2376-2410
-
-
-
42
-
-
35048834773
-
-
J. L. Stymiest, G. Dutheuil, A. Mahmood, V. K. Aggarwal, Angew. Chem. Int. Ed. 2007, 46, 7491–7494;
-
(2007)
Angew. Chem. Int. Ed.
, vol.46
, pp. 7491-7494
-
-
Stymiest, J.L.1
Dutheuil, G.2
Mahmood, A.3
Aggarwal, V.K.4
-
43
-
-
53549103198
-
-
Angew. Chem. 2007, 119, 7635–7638;
-
(2007)
Angew. Chem.
, vol.119
, pp. 7635-7638
-
-
-
44
-
-
80054985942
-
-
M. P. Webster, B. M. Partridge, V. K. Aggarwal, Org. Synth. 2011, 88, 247–259;
-
(2011)
Org. Synth.
, vol.88
, pp. 247-259
-
-
Webster, M.P.1
Partridge, B.M.2
Aggarwal, V.K.3
-
45
-
-
77949826633
-
-
M. Althaus, A. Mahmood, J. R. Suárez, S. P. Thomas, V. K. Aggarwal, J. Am. Chem. Soc. 2010, 132, 4025–4028;
-
(2010)
J. Am. Chem. Soc.
, vol.132
, pp. 4025-4028
-
-
Althaus, M.1
Mahmood, A.2
Suárez, J.R.3
Thomas, S.P.4
Aggarwal, V.K.5
-
46
-
-
84899446404
-
-
A. P. Pulis, P. Fackler, V. K. Aggarwal, Angew. Chem. Int. Ed. 2014, 53, 4382–4385;
-
(2014)
Angew. Chem. Int. Ed.
, vol.53
, pp. 4382-4385
-
-
Pulis, A.P.1
Fackler, P.2
Aggarwal, V.K.3
-
47
-
-
84908085024
-
-
Angew. Chem. 2014, 126, 4471–4474;
-
(2014)
Angew. Chem.
, vol.126
, pp. 4471-4474
-
-
-
48
-
-
84954451112
-
-
A. Millán, J. R. Smith, J. L.-Y. Chen, V. K. Aggarwal, Angew. Chem. Int. Ed. 2016, 55, 2498–2502;
-
(2016)
Angew. Chem. Int. Ed.
, vol.55
, pp. 2498-2502
-
-
Millán, A.1
Smith, J.R.2
Chen, J.L.-Y.3
Aggarwal, V.K.4
-
49
-
-
85003726153
-
-
Angew. Chem. 2016, 128, 2544–2548;
-
(2016)
Angew. Chem.
, vol.128
, pp. 2544-2548
-
-
-
51
-
-
53249098863
-
-
H. Lange, R. Huenerbein, B. Wibbeling, R. Fröhlich, S. Grimme, D. Hoppe, Synthesis 2008, 2905–2918;
-
(2008)
Synthesis
, pp. 2905-2918
-
-
Lange, H.1
Huenerbein, R.2
Wibbeling, B.3
Fröhlich, R.4
Grimme, S.5
Hoppe, D.6
-
52
-
-
48549104017
-
-
H. Lange, R. Huenerbein, R. Fröhlich, S. Grimme, D. Hoppe, Chem. Asian J. 2008, 3, 78–87.
-
(2008)
Chem. Asian J.
, vol.3
, pp. 78-87
-
-
Lange, H.1
Huenerbein, R.2
Fröhlich, R.3
Grimme, S.4
Hoppe, D.5
-
53
-
-
85043910605
-
-
For enantioselective lithiation–borylations with lithiated primary benzyl carbamates, see
-
For enantioselective lithiation–borylations with lithiated primary benzyl carbamates, see:
-
-
-
-
54
-
-
84899566051
-
-
S. C. Matthew, B. W. Glasspoole, O. Eisenberger, C. M. Crudden, J. Am. Chem. Soc. 2014, 136, 5828–5831;
-
(2014)
J. Am. Chem. Soc.
, vol.136
, pp. 5828-5831
-
-
Matthew, S.C.1
Glasspoole, B.W.2
Eisenberger, O.3
Crudden, C.M.4
-
55
-
-
84891030906
-
-
for boronic ester homologation with configurationally labile α-silyl carbamates, see
-
L. Chausset-Boissarie, K. Ghozati, E. LaBine, J. L.-Y. Chen, V. K. Aggarwal, C. M. Crudden, Chem. Eur. J. 2013, 19, 17698–17701; for boronic ester homologation with configurationally labile α-silyl carbamates, see:
-
(2013)
Chem. Eur. J.
, vol.19
, pp. 17698-17701
-
-
Chausset-Boissarie, L.1
Ghozati, K.2
LaBine, E.3
Chen, J.L.-Y.4
Aggarwal, V.K.5
Crudden, C.M.6
-
56
-
-
84925067735
-
-
A. L. Barsamian, Z. Wu, P. R. Blakemore, Org. Biomol. Chem. 2015, 13, 3781–3786.
-
(2015)
Org. Biomol. Chem.
, vol.13
, pp. 3781-3786
-
-
Barsamian, A.L.1
Wu, Z.2
Blakemore, P.R.3
-
57
-
-
85043903432
-
-
For stereospecific Suzuki cross-couplings of secondary benzylic boronic esters with retention of chirality, see
-
For stereospecific Suzuki cross-couplings of secondary benzylic boronic esters with retention of chirality, see:
-
-
-
-
58
-
-
67749113467
-
-
D. Imao, B. W. Glasspoole, V. S. Laberge, C. M. Crudden, J. Am. Chem. Soc. 2009, 131, 5024–5025;
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 5024-5025
-
-
Imao, D.1
Glasspoole, B.W.2
Laberge, V.S.3
Crudden, C.M.4
-
59
-
-
84879499332
-
-
B. W. Glasspoole, M. S. Oderinde, B. D. Moore, A. Antoft-Finch, C. M. Crudden, Synthesis 2013, 45, 1759–1763;
-
(2013)
Synthesis
, vol.45
, pp. 1759-1763
-
-
Glasspoole, B.W.1
Oderinde, M.S.2
Moore, B.D.3
Antoft-Finch, A.4
Crudden, C.M.5
-
60
-
-
85043914431
-
-
see reference [13b];
-
see reference [13b];
-
-
-
-
61
-
-
84962639328
-
-
C. M. Crudden, C. Ziebenhaus, J. P. G. Rygus, K. Ghozati, P. J. Unsworth, M. Nambo, S. Voth, M. Hutchinson, V. S. Laberge, Y. Maekawa, D. Imao, Nat. Commun. 2016, 7, 11065.
-
(2016)
Nat. Commun.
, vol.7
, pp. 11065
-
-
Crudden, C.M.1
Ziebenhaus, C.2
Rygus, J.P.G.3
Ghozati, K.4
Unsworth, P.J.5
Nambo, M.6
Voth, S.7
Hutchinson, M.8
Laberge, V.S.9
Maekawa, Y.10
Imao, D.11
-
62
-
-
0000755451
-
-
G. Zweifel, H. Arzoumanian, C. C. Whitney, J. Am. Chem. Soc. 1967, 89, 3652–3653;
-
(1967)
J. Am. Chem. Soc.
, vol.89
, pp. 3652-3653
-
-
Zweifel, G.1
Arzoumanian, H.2
Whitney, C.C.3
-
63
-
-
0017043244
-
-
D. A. Evans, T. C. Crawford, R. C. Thomas, J. A. Walker, J. Org. Chem. 1976, 41, 3947–3953;
-
(1976)
J. Org. Chem.
, vol.41
, pp. 3947-3953
-
-
Evans, D.A.1
Crawford, T.C.2
Thomas, R.C.3
Walker, J.A.4
-
65
-
-
81555210062
-
-
S. Xu, C.-T. Lee, H. Rao, E. Negishi, Adv. Synth. Catal. 2011, 353, 2981–2987.
-
(2011)
Adv. Synth. Catal.
, vol.353
, pp. 2981-2987
-
-
Xu, S.1
Lee, C.-T.2
Rao, H.3
Negishi, E.4
-
66
-
-
84962236812
-
-
Y. Wang, A. Noble, E. L. Myers, V. K. Aggarwal, Angew. Chem. Int. Ed. 2016, 55, 4270–4274;
-
(2016)
Angew. Chem. Int. Ed.
, vol.55
, pp. 4270-4274
-
-
Wang, Y.1
Noble, A.2
Myers, E.L.3
Aggarwal, V.K.4
-
67
-
-
85003640307
-
-
Angew. Chem. 2016, 128, 4342–4346.
-
(2016)
Angew. Chem.
, vol.128
, pp. 4342-4346
-
-
-
68
-
-
33845377563
-
-
E. Negishi, D. E. Van Horn, T. Yoshida, J. Am. Chem. Soc. 1985, 107, 6639–6647;
-
(1985)
J. Am. Chem. Soc.
, vol.107
, pp. 6639-6647
-
-
Negishi, E.1
Van Horn, D.E.2
Yoshida, T.3
-
70
-
-
0006160669
-
-
Angew. Chem. 1993, 105, 1095–1097;
-
(1993)
Angew. Chem.
, vol.105
, pp. 1095-1097
-
-
-
73
-
-
85043964716
-
-
Transesterification to the pinacol boronic ester greatly facilitated isolation of the product due to the greater stability compared to the neopentyl glycol derivative.
-
Transesterification to the pinacol boronic ester greatly facilitated isolation of the product due to the greater stability compared to the neopentyl glycol derivative.
-
-
-
-
74
-
-
85043913309
-
-
Relative configuration determined by completion of the synthesis of 3-epi-tatanan A.
-
Relative configuration determined by completion of the synthesis of 3-epi-tatanan A.
-
-
-
-
75
-
-
85043883441
-
-
See the Supporting Information for details.
-
See the Supporting Information for details.
-
-
-
-
76
-
-
84907943523
-
-
L. Li, A. Joshi-Pangu, M. Diane, M. R. Biscoe, J. Am. Chem. Soc. 2014, 136, 14027–14030.
-
(2014)
J. Am. Chem. Soc.
, vol.136
, pp. 14027-14030
-
-
Li, L.1
Joshi-Pangu, A.2
Diane, M.3
Biscoe, M.R.4
-
79
-
-
0029995822
-
-
D. S. Matteson, H.-W. Man, O. C. Ho, J. Am. Chem. Soc. 1996, 118, 4560–4566;
-
(1996)
J. Am. Chem. Soc.
, vol.118
, pp. 4560-4566
-
-
Matteson, D.S.1
Man, H.-W.2
Ho, O.C.3
-
80
-
-
0000189831
-
-
for selected reviews, see
-
D. J. S. Tsai, D. S. Matteson, Organometallics 1983, 2, 236–241; for selected reviews, see:
-
(1983)
Organometallics
, vol.2
, pp. 236-241
-
-
Tsai, D.J.S.1
Matteson, D.S.2
-
81
-
-
61349161740
-
-
S. P. Thomas, R. M. French, V. Jheengut, V. K. Aggarwal, Chem. Rec. 2009, 9, 24–39;
-
(2009)
Chem. Rec.
, vol.9
, pp. 24-39
-
-
Thomas, S.P.1
French, R.M.2
Jheengut, V.3
Aggarwal, V.K.4
|