Academic literature on the topic 'N,S-acetals'

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Journal articles on the topic "N,S-acetals"

1

Schuijl, P. J. W., H. J. T. Bos, and L. Brandsma. "Ketene S,N-acetals from thioamides." Recueil des Travaux Chimiques des Pays-Bas 87, no. 1 (2010): 123–25. http://dx.doi.org/10.1002/recl.19680870116.

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2

Junjappa, H., H. Ila та C. V. Asokan. "α-Oxoketene-S,S-, N,S- and N,N-acetals: Versatile intermediates in organic synthesis". Tetrahedron 46, № 16 (1990): 5423–506. http://dx.doi.org/10.1016/s0040-4020(01)87748-6.

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3

TAKAHATA, HIROKI, TOMOKO NAKAJIMA, MASAHARU NAKANO, AKIRA TOMIGUCHI, and TAKAO YAMAZAKI. "Ketene-S,N-acetals as synthetic intermediates for heterocycles. Reaction of ketene-S,N-acetals with aryl isocyanates." CHEMICAL & PHARMACEUTICAL BULLETIN 33, no. 10 (1985): 4299–308. http://dx.doi.org/10.1248/cpb.33.4299.

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4

Mathews, Annie, E. R. Anabha, and C. G. Sholly. "A Facile Method for the Synthesis of Oxoketene-N,S- and -N,N-acetals from Reactions of Amino Compounds." Organic Chemistry International 2010 (November 28, 2010): 1–5. http://dx.doi.org/10.1155/2010/396020.

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Abstract:
2-Aroyl-3,3-bis(alkylsulfanyl)acrylaldehydes reacted with various primary amines, namely, o-phenylenediamine, ethylenediamine, and anilines to produce functionalized oxoketene-N,S-acetals and N,N-acetals in good yields. Imidazolo derivatives synthesized with o-phenylenediamine and ethylenediamine containing a formyl group could act as valuable starting materials for a variety of substituted heterocyclic compounds.
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5

Rudoref, Wolf-Dieter, Jens Köditz, Nadja Henze, and Ani Tersakian. "REACTIONS OF ACYLFORMYLKETENE S,S-AND S,N-ACETALS WITH AMINES." Phosphorus, Sulfur, and Silicon and the Related Elements 107, no. 1-4 (1995): 87–97. http://dx.doi.org/10.1080/10426509508027924.

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6

Hojo, Masaru, Ryōichi Masuda, Etsuji Okada, Hiromi Yamamoto, Katsushi Morimoto та Ken Okada. "Facile Synthesis of β-TrifluoroacetylketeneO,N-,S,N- andN,N-Acetals". Synthesis 1990, № 03 (1990): 195–98. http://dx.doi.org/10.1055/s-1990-26827.

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7

OTTEN, P. A., N. OSKAM, and A. VAN DER GEN. "ChemInform Abstract: A Horner-Wittig Approach to S,N-Ketene Acetals. Acid-Catalyzed Hydrolysis of S,N-Ketene Acetals to (S)-Thioesters." ChemInform 27, no. 50 (2010): no. http://dx.doi.org/10.1002/chin.199650075.

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8

Zhang, Lin, Jinhuan Dong, Xianxiu Xu, and Qun Liu. "Chemistry of Ketene N,S-Acetals: An Overview." Chemical Reviews 116, no. 2 (2016): 287–322. http://dx.doi.org/10.1021/acs.chemrev.5b00360.

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9

Kirkeby, Emily K., and Andrew G. Roberts. "Design, synthesis and characterization of structurally dynamic cyclic N,S-acetals." Chemical Communications 56, no. 64 (2020): 9118–21. http://dx.doi.org/10.1039/d0cc03503c.

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10

El-Saghier, Ahmed M. M., Mansour A. Makhlouf, Naglaa F. H. Mahmoud, and Wedad A. El-Adawish. "A-Alkenoyl Ketene S,S- and N,S-Acetals As Starting For Unexpected and Novel Synthesis of N-Heterocycles." JOURNAL OF ADVANCES IN CHEMISTRY 6, no. 1 (2010): 861–72. http://dx.doi.org/10.24297/jac.v6i1.965.

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Abstract:
A series of N-heterocycles such as diazaspiro-[4.5]decane, pyrazolo[4,3-d][1,2]-diazepine, imidazo[3,2,1ij][1,8]naphthyridine derivatives or pyrazolo[3,4-b]pyridin-4-ol were synthesized using a-alkenoyl-, a,a-dialkenoyl ketene-(S,S)-acetals 2a-d, 3a-c or a-dialkenoyl ketene-(N,S)-acetal 12 as starting materials. The biological activity of some new synthesized compounds have been investigated.
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