275. Guo Z, Ngooi TK, Scilimati A, Fülling G, Sih CJ (1988) Tetrahedron Lett. 29: 5583
276. Gutman AL, Zuobi K, Boltansky A (1987) Tetrahedron Lett. 28: 3861
277. Henkel B, Kunath A, Schick H (1993) Tetrahedron Asymmetry 4: 153
278. Zhang Y, Schaufelberger F, Sakulsombat M, Liu C, Ramstr€ om O (2014) Tetrahedron 70:
3826.
279. Guo Z, Sih CJ (1988) J. Am. Chem. Soc. 110: 1999
280. Ngooi TK, Scilimati A, Guo Z-W, Sih CJ (1989) J. Org. Chem. 54: 911
281. Lobell M, Schneider MP (1993) Tetrahedron Asymmetry 4: 1027
282. Barker CV, Page MI, Korn SR, Monteith M (1999) Chem. Commun. 721.
283. Gutman AL, Meyer E, Yue X, Abell C (1992) Tetrahedron Lett. 33: 3943.
284. Gotor V (1992) Enzymatic aminolysis, hydrazinolysis and oximolysis reactions. In: Servi S
(ed) Microbial Reagents in Organic Synthesis. Kluwer, Dordrecht, p 199
285. Garcia MJ, Rebolledo F, Gotor V (1993) Tetrahedron Lett. 34: 6141
286. Chen ST, Jang MK, Wang KT (1993) Synthesis. 858
287. Gotor V, Brieva R, Gonzalez C, Rebolledo F (1991) Tetrahedron 47: 9207
288. Rebolledo F, Brieva R, Gotor V (1989) Tetrahedron Lett. 30: 5345
289. Fastrez J, Fersht AR (1973) Biochemistry 12: 2025
290. Yagisawa S (1981) J. Biochem. (Tokyo) 89: 491
291. Astorga C, Rebolledo F, Gotor V (1991) Synthesis. 350
292. Al-Mulla EAJ, Yunus WMZW, Ibrahim NAB, Rahman MZA (2010) J. Oleo. Sci. 59: 59.
293. Bruggink A, Roos EC, De Vroom E (1998) Org. Proc. Res. Dev. 2: 128.
294. de Zoete MC, Kock-van Dalen AC, van Rantwijk F, Sheldon RA (1993) J. Chem. Soc. Chem.
Commun. 1831
295. Gotor V, Brieva R, Rebolledo F (1988) J. Chem. Soc. Chem. Commun. 957
296. Balkenhohl F, Dietrich K, Hauer B, Ladner W (1997) J. Prakt. Chem. 339: 381
297. Messina F, Botta M, Corelli F, Schneider MP, Fazio F (1999) J. Org. Chem. 64: 3767
298. Roche D, Prasad K, Repic O (1999) Tetrahedron Lett. 40: 3665
299. Brieva R, Rebolledo F, Gotor V (1990) J. Chem. Soc. Chem. Commun. 1386
300. Takayama S, Lee ST, Chung SC, Wong CH (1999) Chem. Commun. 127
301. Ladner WE, Ditrich K (1999) Chimica Oggi, July/August, 51
302. Orsat B, Alper PB, Moree W, Mak CP, Wong CH (1996) J. Am. Chem. Soc. 118: 712
303. van Rantwijk F, Sheldon RA (2004) Tetrahedron 60: 501
304. Smidt H, Fischer A, Fischer P, Schmidt RD (1996) Biotechnol. Tech. 10: 335
305. Ahn Y, Ko S-B, Kim M-J, Park J, (2008) Coord. Chem. Rev. 252: 647.
306. Parvulescu A, Janssens J, Vanderleyden J, Vos D (2010) Top. Catal. 53: 931.
307. Reetz MT, Schimossek K (1996) Chimia 50: 668
308. Parvulescu A, De Vos D, Jacobs P (2005) Chem. Commun. 5307
309. Pamies O, Ell AH, Samec JSM, Hermanns N, Ba ¨ckvall JE (2002) Tetrahedron Lett. 43: 4699
310. Paetzold J, Ba ¨ckvall JE (2005) J. Am. Chem. Soc. 127: 17620
311. Parvulescu AN, Jacobs PA, De Vos DE (2008) Adv. Synth. Catal. 350: 113
312. Livingston AG, Roengpithya C, Patterson D A, Irwin JL, Parrett MR, Taylor PC (2007)
Chem. Commun. 3462
313. Shakeri M, Tai C, Goethelid E, Oscarsson S, Baeckvall, Jan-E (2011) Chem. Eur. J. 17:
13269.
314. Engstr€ om K, Johnston EV. Verho O, Gustafson KPJ, Shakeri M, Tai C-W, Ba ¨ckvall J-E
(2016) Angew. Chem. Int. Ed. 52: 14006.
315. Pamies Oscar, Ell AH, Samec JSM, Hermanns N, Backvall, Jan-E (2002) Tetrahedron Lett.
43: 4699.
316. Stirling MJ, Mwansa JM, Sweeney G, Blacker AJ, Page MI (2016) Org. Biomol. Chem. 14:
7092.
317. Gastaldi S, Escoubet S, Vanthuyne N, Gil G, Bertrand MP (2007) Org. Lett. 9: 837.
318. Ding W, Li M, Deng Y (2012) Tetrahedron: Asymm. 23: 1376.
319. O ¨ hrner N, Orrenius C, Mattson A, Norin T, Hult K (1996) Enzyme Microb. Technol. 19: 328
396
3 Special Techniques
276. Gutman AL, Zuobi K, Boltansky A (1987) Tetrahedron Lett. 28: 3861
277. Henkel B, Kunath A, Schick H (1993) Tetrahedron Asymmetry 4: 153
278. Zhang Y, Schaufelberger F, Sakulsombat M, Liu C, Ramstr€ om O (2014) Tetrahedron 70:
3826.
279. Guo Z, Sih CJ (1988) J. Am. Chem. Soc. 110: 1999
280. Ngooi TK, Scilimati A, Guo Z-W, Sih CJ (1989) J. Org. Chem. 54: 911
281. Lobell M, Schneider MP (1993) Tetrahedron Asymmetry 4: 1027
282. Barker CV, Page MI, Korn SR, Monteith M (1999) Chem. Commun. 721.
283. Gutman AL, Meyer E, Yue X, Abell C (1992) Tetrahedron Lett. 33: 3943.
284. Gotor V (1992) Enzymatic aminolysis, hydrazinolysis and oximolysis reactions. In: Servi S
(ed) Microbial Reagents in Organic Synthesis. Kluwer, Dordrecht, p 199
285. Garcia MJ, Rebolledo F, Gotor V (1993) Tetrahedron Lett. 34: 6141
286. Chen ST, Jang MK, Wang KT (1993) Synthesis. 858
287. Gotor V, Brieva R, Gonzalez C, Rebolledo F (1991) Tetrahedron 47: 9207
288. Rebolledo F, Brieva R, Gotor V (1989) Tetrahedron Lett. 30: 5345
289. Fastrez J, Fersht AR (1973) Biochemistry 12: 2025
290. Yagisawa S (1981) J. Biochem. (Tokyo) 89: 491
291. Astorga C, Rebolledo F, Gotor V (1991) Synthesis. 350
292. Al-Mulla EAJ, Yunus WMZW, Ibrahim NAB, Rahman MZA (2010) J. Oleo. Sci. 59: 59.
293. Bruggink A, Roos EC, De Vroom E (1998) Org. Proc. Res. Dev. 2: 128.
294. de Zoete MC, Kock-van Dalen AC, van Rantwijk F, Sheldon RA (1993) J. Chem. Soc. Chem.
Commun. 1831
295. Gotor V, Brieva R, Rebolledo F (1988) J. Chem. Soc. Chem. Commun. 957
296. Balkenhohl F, Dietrich K, Hauer B, Ladner W (1997) J. Prakt. Chem. 339: 381
297. Messina F, Botta M, Corelli F, Schneider MP, Fazio F (1999) J. Org. Chem. 64: 3767
298. Roche D, Prasad K, Repic O (1999) Tetrahedron Lett. 40: 3665
299. Brieva R, Rebolledo F, Gotor V (1990) J. Chem. Soc. Chem. Commun. 1386
300. Takayama S, Lee ST, Chung SC, Wong CH (1999) Chem. Commun. 127
301. Ladner WE, Ditrich K (1999) Chimica Oggi, July/August, 51
302. Orsat B, Alper PB, Moree W, Mak CP, Wong CH (1996) J. Am. Chem. Soc. 118: 712
303. van Rantwijk F, Sheldon RA (2004) Tetrahedron 60: 501
304. Smidt H, Fischer A, Fischer P, Schmidt RD (1996) Biotechnol. Tech. 10: 335
305. Ahn Y, Ko S-B, Kim M-J, Park J, (2008) Coord. Chem. Rev. 252: 647.
306. Parvulescu A, Janssens J, Vanderleyden J, Vos D (2010) Top. Catal. 53: 931.
307. Reetz MT, Schimossek K (1996) Chimia 50: 668
308. Parvulescu A, De Vos D, Jacobs P (2005) Chem. Commun. 5307
309. Pamies O, Ell AH, Samec JSM, Hermanns N, Ba ¨ckvall JE (2002) Tetrahedron Lett. 43: 4699
310. Paetzold J, Ba ¨ckvall JE (2005) J. Am. Chem. Soc. 127: 17620
311. Parvulescu AN, Jacobs PA, De Vos DE (2008) Adv. Synth. Catal. 350: 113
312. Livingston AG, Roengpithya C, Patterson D A, Irwin JL, Parrett MR, Taylor PC (2007)
Chem. Commun. 3462
313. Shakeri M, Tai C, Goethelid E, Oscarsson S, Baeckvall, Jan-E (2011) Chem. Eur. J. 17:
13269.
314. Engstr€ om K, Johnston EV. Verho O, Gustafson KPJ, Shakeri M, Tai C-W, Ba ¨ckvall J-E
(2016) Angew. Chem. Int. Ed. 52: 14006.
315. Pamies Oscar, Ell AH, Samec JSM, Hermanns N, Backvall, Jan-E (2002) Tetrahedron Lett.
43: 4699.
316. Stirling MJ, Mwansa JM, Sweeney G, Blacker AJ, Page MI (2016) Org. Biomol. Chem. 14:
7092.
317. Gastaldi S, Escoubet S, Vanthuyne N, Gil G, Bertrand MP (2007) Org. Lett. 9: 837.
318. Ding W, Li M, Deng Y (2012) Tetrahedron: Asymm. 23: 1376.
319. O ¨ hrner N, Orrenius C, Mattson A, Norin T, Hult K (1996) Enzyme Microb. Technol. 19: 328
396
3 Special Techniques