Gassman Indole Synthesis Essay

(1) Kawasaki T, Higuchi K. Nat. Prod. Rep. 2005;22:761–793.[PubMed]

(2) Walsh TF, Toupence RB, Ujjainwalla F, Young JR, Goulet MT. Tetrahedron. 2001;57:5233–5241.

(3) Watson TJN, Horgan SW, Shah RS, Farr RA, Schnettler RA, Nevill CR, Weiberth FJ, Huber EW, Baron BM, Webster ME, Mishra RJ, Harrison BL, Nyce PL, Rand CL, Gorlaski CT. Org. Process Res. Dev. 2000;4:477–487.

(4) Jacotot B, Banga JD, Pfister P, Mehra M. Br. J. Clin. Pharmac. 1994;38:257–263.[PMC free article][PubMed]

(5) (a) Brown RK. In: Indoles Part One. Houlihan WJ, editor. Wiley; New York: 1972. pp. 227–559. (b) Sundberg R. Indoles. Academic Press; San Diego: 1996. pp. 7–53. (c) Humphrey GR, Kuethe JT. Chem. Rev. 2006;106:2875–2911.[PubMed]

(6) Gribble GW. J. Chem. Soc., Perkin Trans. 1. 2000:1045–1075.

(7) Robinson B. The Fischer Indole Synthesis. Wiley-Interscience; New York: 1982.

(8) Clark RD, Repke DH. Heterocycles. 1984;63:214–221.

(9) Castro CE, Stephens RD. J. Org. Chem. 1963;28:2163.

(10) Nenitzescu CD. Bull. Soc. Chim. Romania. 1929;11:37–43.

(11) Kurti L, Czako B. Strategic Applications of Named Reactions in Organic Synthesis. Elsevier; London: 2005. pp. 172–173.

(12) Söderberg BC, Chisnell AC, O'Neil SN, Shriver JA. J. Org. Chem. 1999;64:9731–9734.

(13) (a) Cadogan JIG, Cameron-Wood M. Proc. Chem. Soc. 1962:361. (b) Cadogan JIG, Mackie RK, Todd MJ. J. Chem. Soc., Chem. Comm. 1966:491.

(14) (a) Sundberg RJ. J. Org. Chem. 1965;30:3604–3610. (b) Sundberg RJ, Tamazaki T. J. Org. Chem. 1967;32:290–294.

(15) Cacchi S, Fabrizi G. Chem. Rev. 2005;105:2873–2920.[PubMed]

(16) Fukuyama T, Chen X, Peng G. J. Am. Chem. Soc. 1994;116:3127–3128.

(17) Fürstner A, Hupperts A. J. Am. Chem. Soc. 1995;117:4468–4475.

(18) Fuwa H, Sasaki M. Org. Biomol. Chem. 2007;5:2214–2218.[PubMed]

(19) (a) Arcadi A, Cacchi S, Marinelli F. Tetrahedron Lett. 1992;33:3915–3918. (b) Lu BZ, Zhao W, Wei H, Dufour M, Farina V, Senanayake CH. Org. Lett. 2006;8:3271–3274.[PubMed]

(20) Zeni G, Larock RC. Chem. Rev. 2004;104:2285–2309. Reviews. [PubMed] (b) Larock RC. Top. Organomet. Chem. 2005;14:147–182.

(21) Larock RC, Yum EK. J. Am. Chem. Soc. 1991;113:6689–6690.

(22) Larock RC, Yum EK, Refvik MD. J. Org. Chem. 1998;63:7652–7662.

(23) Nishikawa T, Wada K, Isobe M. Biosci. Biotechnol. Biochem. 2002;66:2273–2278.[PubMed]

(24) Roschanger F, Liu J, Estanove E, Dufour M, Rodriguez S, Farina V, Hickey E, Hossain A, Jones PJ, Lee H, Lu BZ, Varsolona R, Schroder J, Beaulieu P, Gillard J, Senanayake CH. Tetrahedron Lett. 2008;49:363–366.

(25) (a) Brodfuehrer PR, Chen BC, Sattelberg TR, Smith PR, Reddy JP, Stark DR, Quinlan SL, Reid JG, Thottathil JK, Wang SJ. J. Org. Chem. 1997;62:9192–9202. (b) Chen C, Lieberman DR, Larsen RD, Reamer RA, Verhoeven TR, Reider PJ. Tetrahedron Lett. 1994;35:6981–6984.

(26) Kurti L, Czako B. Strategic Applications of Named Reactions in Organic Synthesis. Elsevier; London: 2005. pp. 260–261.

(27) (a) Denmark SE, Baird JD. Org. Lett. 2004;6:3649–3652.[PubMed] (b) Denmark SE, Baird JD. Org. Lett. 2006;8:793–795.[PubMed] (c) Denmark SE, Baird JD, Regens CS. J. Org. Chem. 2008;73:1440–1455.[PubMed]

(28) (a)

* Corresponding authors

a School of Chemistry and Chemical Engineering and Jiangsu Key Laboratory of Green Synthetic Chemistry for Functional Materials, Jiangsu Normal University, Xuzhou, P. R. China
E-mail:yhshi@jsnu.edu.cn
Tel: +86 516 8350 0349

b State Key Laboratory of Coordination Chemistry, Nanjing University, Nanjing, P. R. China

c State Key Laboratory of Inorganic Synthesis and Preparative Chemistry, Jilin University, Changchun, P. R. China

One thought on “Gassman Indole Synthesis Essay

Leave a Reply

Your email address will not be published. Required fields are marked *