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N-tの部分一致の例文一覧と使い方

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例文

1.%C, %N, %S, %T, %Lor%C, %N, %S, %T, %l, %t, %c2.%C, %N, %S, %T, %l3.%C, %N, %S, %T4.%N, %S, %T, %Lor%N, %S, %T, %l, %t, %c5.%N, %S, %T, %l6.%N, %S, %T 例文帳に追加

パスにおける6つのエントリーの順序は上記のままでなければならない。 - XFree86

These entries must contain the following substitutions: 例文帳に追加

このエントリーは以下の置き換えを含まなければならない:1. %C, %N, %S, %T, %L または %C, %N, %S, %T, %l, %t, %c2. %C, %N, %S, %T, %l3. %C, %N, %S, %T4. %N, %S, %T, %L または %N, %S, %T, %l, %t, %c5. %N, %S, %T, %l6. %N, %S, %T - XFree86

例文

By using the t(2), N(0)t(2) is processed.例文帳に追加

このｔ（２）を用いて、Ｎ（０）ｔ（２）の実行を行う。 - 特許庁

Some theory insists that phonemes except for/s, z/ (/k, g/,/t, d/,/n/,/h, b/,/p/,/m/ and/r/) were palatalized. 例文帳に追加

音素/s,z/以外の/k,g/、/t,d/、/n/、/h,b/、/p/、/m/ならびに/r/においては口蓋化があったとする説もある。 - Wikipedia日英京都関連文書対訳コーパス

The method for producing the intermediate from a (2S,4R)-4-alkylsilyloxy-N-t-butoxycarbonylpyrrolidine-2-carbaldehyde derivative through a new crystallizable intermediate (2S,4R)-N-t-butoxycarbonyl-2-[[(3R)-N-t-butoxycarbonylpyrrolidin-3-yl-(R)-hydroxy]methyl]-4-hydroxypyrrolidine by an aldol reaction using an asymmetric assistant such as an amino-alcohol.例文帳に追加

(2S,4R)-4-アルキルシリルオキシ-N-t-ブトキシカルボニルピロリジン-2-カルバルデヒド誘導体からアミノアルコール等の不斉補助剤を使用したアルドール反応より、また結晶性を有する新規な中間体(2S,4R)-N-t-ブトキシカルボニル-2-[[(3R)-N-t-ブトキシカルボニルピロリジン-3-イル-(R)-ヒドロキシ]メチル]-4-ヒドロキシピロリジンを経由して上記の中間体を製造方法とする。 - 特許庁

In the formula, T represents a substituent; L^1 and L^2 each represent a linking group; and n^1 and n^2 each represent 0-30.例文帳に追加

Ｔは置換基、Ｌ^1、Ｌ^2は連結基、ｎ^1、ｎ^2は０〜３０を表す。 - 特許庁

例文

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