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The Preparation ofN-Protected Amino Alcohols andN-Protected Peptide Alcohol by Reduction of the Corresponding Esters with Sodium Borohydride. An Improved Procedure Involving a Slow Addition of a Small Amount of Methanol

机译：通过用硼氢化钠还原相应的酯，通过将相应的酯还原制备保护的氨基醇和受保护的肽醇。一种改进的程序，涉及缓慢添加少量甲醇

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Kenso Soai; Hidekazu Oyamada; Masako Takase;
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年度 1984
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1. Simple methodology for the preparation of amino alcohols from amino acid esters using nabh4-methanol in THF [J] . Goncalves R.S.B., Pinheiro A.C., Da Silva E.T., Synthetic Communications . 2011,第7a9期

机译：在THF中使用Nabh4-甲醇从氨基酸酯制备氨基醇的简单方法
2. Detailed studies on the reduction of aliphatic 3-, 4-, 6-, and 13-oximino esters: Synthesis of novel isomeric amino esters, oximino alcohols, and amino alcohols [J] . Kucuk Hatice Baspinar, Yasa Hasniye, Yildiz Tulay, Synthetic Communications . 2017,第21a24期

机译：关于减少脂族3-，4-，6-和13-羟尼氨基酯的详细研究：新型异构氨基酯的合成，羟基氨基醇和氨基醇
3. Simple Reduction of Heteroaromatic Esters to Alcohols Using a Sodium Borohydride-Methanol System [J] . Nubia Boechat, Jorge Carlos Santos da Costa, Jorge de Souza Mendonca, Synthetic Communications . 2005,第24期

机译：使用硼氢化钠-甲醇系统将杂芳族酯简单还原为醇
4. Sugar Based g-Amino Alcohol Organocatalyst for Enantioselective Michael Addition of β-Keto Esters with Nitroolefins [C] . Divakar Ganesan, Chigusa Seki, Koji Uwai 日本化学会春季年会講演予稿集 . 2018

机译：糖基G-氨基酒精有机催化剂用于对映选择性的迈克尔加入亚硝烯烃的β-酮酯
5. Practical Procedure for the Chemoselective Reduction of Esters by Sodium Borohydride. Effect of the Slow Addition of Methanol [O] . Kenso Soai, Hidekazu Oyamada, Masako Takase, 1984

机译：通过硼氢化钠化学选择性化学选择性的实用方法。缓慢加入甲醇的影响
6. Chiral Synthesis via Organoboranes. 34. Selective Reductions. 47. AsymmetricReduction of Hindered Alpha, Beta-Acetylenic Ketones with B-Chlorodiisopinocampheylborane to Propargylic Alcohols of Very High Enantiomeric Excess. Improved Workup Procedure for t [R] . Ramachandran, P. V., Teodorovic, A. V., Rangaishenvi, M. V., 1992

机译：有机硼烷的手性合成。 34.选择性削减。 47.受阻的α，β-炔酮与B-氯二异庚基硼烷不对称还原为极高对映体过量的炔丙醇。改进了t的处理程序

The Preparation ofN-Protected Amino Alcohols andN-Protected Peptide Alcohol by Reduction of the Corresponding Esters with Sodium Borohydride. An Improved Procedure Involving a Slow Addition of a Small Amount of Methanol

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