J. W. Daly, I. Karle, C. W. Myers, T. Tokuyama, J. A. Waters et al., Proc. Nat. Acad. Sci. USA, vol.68, pp.1870-1875, 1971.

T. F. Spande, H. M. Garraffo, J. W. Daly, T. Tokuyama, A. Shimada et al., Tetrahedron, vol.48, pp.3453-3460, 1986.

J. W. Daly and T. F. Spande, Alkaloids: Chemical and Biological Perspectives, vol.4, pp.36-92, 1986.

T. H. Jones, R. M. Adams, T. F. Spande, H. M. Garraffo, T. Kaneko et al., J. Nat. Prod, vol.75, pp.1930-1936, 2012.

C. Eldridge, G. Quek, M. Sako, J. H. Ryan, S. Saubern et al., Proc. Nat. Acad. Sci. USA, vol.74, pp.2172-2176, 1977.

:. A. Sinclair and R. A. Stockman, Nat. Prod. Rep, vol.24, pp.298-326, 2007.

K. Matsumura, K. Nishikawa, H. Yoshida, M. Doe, Y. Morimoto et al., , vol.8, pp.11296-11303, 2018.

N. D. Spiccia, J. Burnley, K. Subasinghe, C. Perry, L. Lefort et al., J. Org. Chem, vol.82, pp.8725-8732, 2017.

M. Sato, H. Azuma, A. Daigaku, S. Sato, K. Takasu et al., Angew. Chem. Int. Ed, vol.56, pp.1087-1091, 2017.

. Angew and . Chem, , vol.129, pp.4237-4245, 2016.

E. H. Krenske, S. Agopcan, V. Aviyente, K. N. Houk, B. A. Johnson et al., Org. Biomol. Chem, vol.134, pp.4227-4229, 2008.

Y. Adachi, N. Kamei, S. Yokoshima, and T. Fukuyama, Org. Lett, vol.13, pp.4446-4449, 2011.

S. C. Coote, S. P. Moore, P. O'brien, A. C. Whitwood, and J. Gilday, J. Org. Chem, vol.73, pp.7852-7855, 2008.

J. Zhu, J. Royer, J. Quirion, and H. Husson, Tetrahedron Lett, vol.32, pp.2485-2488, 1991.

N. Girard, L. Pouchain, J. Hurvois, and C. Moinet, Synlett, vol.11, pp.1679-1682, 2006.

M. D. Kärkäs, ;. M. Yan, Y. Kawamata, and P. Baran, For recent reviews on the general aspects of synthetic electrochemistry, see: (a), vol.47, pp.13230-13319, 2017.

M. Möhle, E. Zirbes, T. Rodrigo, A. Gieshoff, S. R. Wiebe et al., Angew. Chem. Int. Ed, vol.57, pp.6018-6041, 2018.

. Angew and . Chem, , vol.130, pp.6124-6149, 2018.

, Typically, the silica/product mass ratio should not exceed 20:1. The optical rotation should be recorded in benzene, and NMR characterization in d6-benzene

A. Toro, P. Nowak, and P. Deslongchamps, J. Am. Chem. Soc, vol.122, pp.3418-3432, 1985.

A. R. Rovira, A. Fin, and Y. Tor, Chem. Sci, vol.8, pp.2983-2993, 2017.

L. Le-corre, L. Tak-tak, A. Guillard, G. Prestat, C. Gravier-pelletier et al., Org. Biomol. Chem, vol.13, pp.409-423, 2015.

B. Dansou, C. Pichon, R. Dhal, E. Brown, and S. Mille, Eur. J. Org. Chem, pp.1527-1533, 2000.

M. Luyten and R. Keese, Tetrahedron, vol.42, pp.1687-1691, 1986.

J. T. Linders, J. L. Flippen-anderson, C. F. George, K. C. Rice, ;. L. Lu et al., Tetrahedron Lett, vol.40, pp.6993-6996, 1989.

H. Takaya, T. Naota, and S. Murahashi, J. Am. Chem. Soc, vol.120, pp.4244-4245, 1998.

R. Malassene, E. Vanquelef, L. Toupet, J. Hurvois, and C. Moinet, Org. Biomol. Chem, vol.1, pp.547-551, 2003.

H. Liu, T. W. Ly, C. Tai, J. Wu, J. Liang et al., Tetrahedron, vol.59, pp.1209-1226, 2003.

P. Compain, J. Goré, and J. Vatèle, Tetrahedron, vol.52, pp.6647-6664, 1996.

J. Terao, H. Todo, S. A. Begum, H. Kuniyasu, and N. Kambe, Angew. Chem. Int. Ed, vol.46, pp.2086-2089, 2007.

. Angew and . Chem, , vol.119, pp.2132-2135, 2007.

B. Carroll, D. G. Kubler, H. W. Davis, and A. M. Whaley, J. Am. Chem. Soc, vol.73, pp.1270-1278, 1951.

J. Dormoy and B. Castro, In: Triphenyl Phosphine Dichloride; e-Eros, Encyclopedia of Reagents for Organic Synthesis, pp.1-4, 2001.

, For the use of Ph3PCl2 as chlorinating agent, see, Tetrahedron Lett, vol.46, pp.229-232, 2005.

L. Horner, H. Oediger, and H. Hoffman, For the reaction of Ph3PCl2/Et3N on cyclohexanone and benzaldehyde, see, Liebigs Ann. Chem, vol.626, pp.26-34, 1959.

R. Webster, A. Boyer, M. J. Fleming, M. Lautens, ;. Takahata et al., For the cyclization of carbamates with adjacent carbon electrophiles, see: (a), vol.12, pp.1587-1575, 2002.

M. Frohn, M. Dalkiewicz, Y. Tu, Z. Wang, and Y. Shi, J. Org. Chem, vol.63, pp.2948-2953, 1998.

A. Alexakis, E. Vrancken, P. Mangeney, and F. Chemla, J. Chem. Soc. Perkin Trans. 1, pp.3352-3353, 2000.

J. Terao, A. Ikumi, H. Kuniyasu, and N. Kambe, J. Am. Chem. Soc, vol.125, pp.5646-5647, 2003.

.. J. Cresswell, S. G. Davies, J. A. Lee, P. M. Roberts, A. J. Russel et al., For a recent SN-1-type epoxide ring opening process, see: A, Org. Lett, vol.12, pp.2936-2939, 2010.

A. Altomare, M. C. Burla, M. Camalli, G. Cascarano, C. Giacovazzo et al., J. Appl. Cryst, vol.32, pp.115-119, 1999.

G. M. Sheldrick and A. Cryst, , vol.64, pp.112-122, 2008.

L. J. Farrugia, J. Appl. Cryst, vol.32, pp.849-854, 2012.