Catalytic Asymmetric Acylation of Alcohols Using a Chiral 1,2‐Diamine Derived from (S)‐Proline: (1S,2S)‐trans‐1‐Benzoyloxy‐2‐bromocyclohexane
Catalytic Asymmetric Acylation of Alcohols Using a Chiral 1,2‐Diamine Derived from (S)‐Proline: (1S,2S)‐trans‐1‐Benzoyloxy‐2‐bromocyclohexane
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DOI：
10.1002/0471264229.os083.11
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发表时间：
2006-04
影响因子：
0.7
通讯作者：
Dai Terakado;T. Oriyama*
中科院分区：
文献类型：
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作者：
Dai Terakado;T. Oriyama*
二叔丁基重碳酸酯-L-异吲哚-1，3-二氢异吲哚二环己基碳二亚胺(S)-N-(N-tert-Butoxycarbonylprolyl)dihydroisoindole反式-2-溴环己醇(S)-1-Methyl-2-[(dihydroisoindol-2-yl)methyl]pyrrolidine(1S，2S)-1-苯甲氧基-2-溴环己烷关键词：不对称酰化；手性二胺；(S)-脯氨酸；醇；有机催化剂；天然产物；外消旋醇；去对称；介孔二醇；废物处理
Di-tert-butyl dicarbonate Tert-Butoxycarbonyl-L-proline Isoindoline 1,3-Dihydroisoindole Dicyclohexylcarbodiimide (S)-N-(N-tert-Butoxycarbonylprolyl)dihydroisoindole Trans-2-Bromocyclohexanol (S)-1-Methyl-2-[(dihydroisoindol-2-yl)methyl]pyrrolidine (1S,2S)-1-Benzoyloxy-2-bromocyclohexane Keywords: asymmetric acylation; chiral diamines; (S)-proline; alcohols; organocatalysts; natural products; racemic alcohols; desymmetrization; meso-diols; waste disposal