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Journal articles on the topic 'Iodolactamization'

Author: Grafiati
Published: 4 June 2021
Last updated: 6 February 2022

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1

Knapp, Spencer, Karen E. Rodriques, Anthony T. Levorse, and Raphael M. Ornaf. "A procedure for “iodolactamization”." Tetrahedron Letters 26, no. 15 (January 1985): 1803–6. http://dx.doi.org/10.1016/s0040-4039(00)94742-7.

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2

Kurth, Mark J., and Steven H. Bloom. "Iodolactamization of .gamma.,.delta.-unsaturated oxazolines." Journal of Organic Chemistry 54, no. 2 (January 1989): 411–14. http://dx.doi.org/10.1021/jo00263a028.

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3

KNAPP, S. "ChemInform Abstract: Iodolactamization: Aspects and Applications." ChemInform 27, no. 36 (August 5, 2010): no. http://dx.doi.org/10.1002/chin.199636270.

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4

Shen, Meihua, and Chaozhong Li. "Asymmetric Iodolactamization Induced by Chiral Oxazolidine Auxiliary." Journal of Organic Chemistry 69, no. 23 (November 2004): 7906–9. http://dx.doi.org/10.1021/jo0488006.

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5

Takahata, Hiroki, Kazuo Yamazaki, Tamotsu Takamatsu, Takao Yamazaki, and Takefumi Momose. "A facile synthesis of N-protected statine and its analog via stereoselective iodolactamization." Journal of Organic Chemistry 55, no. 12 (June 1990): 3947–50. http://dx.doi.org/10.1021/jo00299a045.

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6

Tang, Yu, Ranran Han, Mingcan Lv, Yang Chen, and Pan Yang. "Tandem synthesis of pyrroloisoquinolines through 5-endo iodolactamization, oxidative functionalization and α-amidoalkylation reaction." Tetrahedron 71, no. 25 (June 2015): 4334–43. http://dx.doi.org/10.1016/j.tet.2015.04.057.

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7

Tang, Yu, Ranran Han, Mingcan Lv, Yang Chen, and Pan Yang. "ChemInform Abstract: Tandem Synthesis of Pyrroloisoquinolines Through 5-endo Iodolactamization, Oxidative Functionalization and α-Amidoalkylation Reaction." ChemInform 46, no. 40 (September 17, 2015): no. http://dx.doi.org/10.1002/chin.201540182.

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8

Campbell, Carlton L., Carla Hassler, Soo S. Ko, Matthew E. Voss, Michael A. Guaciaro, Percy H. Carter, and Robert J. Cherney. "Enantioselective Synthesis of Benzyl (1S,2R,4R)-4-(tert-Butoxycarbonylamino)-2-(hydroxymethyl)cyclohexylcarbamate Using an Iodolactamization As the Key Step." Journal of Organic Chemistry 74, no. 16 (August 21, 2009): 6368–70. http://dx.doi.org/10.1021/jo9011249.

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9

Takahata, Hiroki, Tamotsu Takamatsu, Yinshan Chen, Naoki Ohkubo, Takao Yamazaki, Takefumi Momose, and Tadamasa Date. "Electrophilic olefin heterocyclization in organic synthesis. Highly stereoselective synthesis of trans 3,5-disubstituted pyrrolidin-2-ones by iodolactamization via homoallylic asymmetric induction." Journal of Organic Chemistry 55, no. 12 (June 1990): 3792–97. http://dx.doi.org/10.1021/jo00299a019.

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10

KNAPP, S., K. E. RODRIGUES, A. T. LEVORSE, and R. M. ORNAF. "ChemInform Abstract: A PROCEDURE FOR IODOLACTAMIZATION." Chemischer Informationsdienst 16, no. 32 (August 13, 1985). http://dx.doi.org/10.1002/chin.198532154.

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11

Shen, Meihua, and Chaozhong Li. "Asymmetric Iodolactamization Induced by Chiral Oxazolidine Auxiliary." ChemInform 36, no. 12 (March 22, 2005). http://dx.doi.org/10.1002/chin.200512117.

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12

KURTH, M. J., and S. H. BLOOM. "ChemInform Abstract: Iodolactamization of γ,δ-Unsaturated Oxazolines." ChemInform 20, no. 34 (August 22, 1989). http://dx.doi.org/10.1002/chin.198934165.

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13

"IODOLACTAMIZATION: 8-exo-IODO-2-AZABICYCLO[3.3.0]OCTAN-3-ONE." Organic Syntheses 70 (1992): 101. http://dx.doi.org/10.15227/orgsyn.070.0101.

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14

TAKAHATA, H., K. YAMAZAKI, T. TAKAMATSU, T. YAMAZAKI, and T. MOMOSE. "ChemInform Abstract: A Facile Synthesis of N-Protected Statine and Its Analogue via Stereoselective Iodolactamization." ChemInform 21, no. 43 (October 23, 1990). http://dx.doi.org/10.1002/chin.199043264.

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15

TAKAHATA, H., T. TAKAMATSU, Y. S. CHEN, N. OHKUBO, T. YAMAZAKI, T. MOMOSE, and T. DATE. "ChemInform Abstract: Electrophilic Olefin Heterocyclization in Organic Synthesis. Highly Stereoselective Synthesis of trans-3,5-Disubstituted Pyrrolidin-2-ones by Iodolactamization via Homoallylic Asymmetric Induction." ChemInform 21, no. 42 (October 16, 1990). http://dx.doi.org/10.1002/chin.199042190.

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