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Original Articles

Preliminary communication: The synthesis of new mesogenic 1,3,4‐thiadiazole‐2‐carboxylate esters via a novel ring‐closure

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Pages 15-18 | Published online: 04 Aug 2006

Figures & data

Figure 1. Typical mesogenic 1,3,4‐thiadiazoles that have been reported in the literature.

Figure 1. Typical mesogenic 1,3,4‐thiadiazoles that have been reported in the literature.

Figure 2. Cyclization of diacylhydrazides to give 1,3,4‐thiadiazoles.

Figure 2. Cyclization of diacylhydrazides to give 1,3,4‐thiadiazoles.

Figure 3. Tanaka's synthesis of ethyl 5‐phenyl‐2‐thiazolecarboxylate.

Figure 3. Tanaka's synthesis of ethyl 5‐phenyl‐2‐thiazolecarboxylate.

Scheme 1. Synthesis of (S)‐1‐methylheptyl 4‐[5‐(4‐octyloxyphenyl)‐1,3,4‐thiadiazol‐2‐ylcarbonyloxy]benzoate.

Scheme 1. Synthesis of (S)‐1‐methylheptyl 4‐[5‐(4‐octyloxyphenyl)‐1,3,4‐thiadiazol‐2‐ylcarbonyloxy]benzoate.

Scheme 2. Synthesis of (S)‐4‐(1‐methylheptyloxy)phenyl 5‐(4‐dodecyloxyphenyl)‐1,3,4‐thiadiazol‐2‐ylcarboxylate.

Scheme 2. Synthesis of (S)‐4‐(1‐methylheptyloxy)phenyl 5‐(4‐dodecyloxyphenyl)‐1,3,4‐thiadiazol‐2‐ylcarboxylate.

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