PREPARATION AND REACTION OF NOVEL OXYGEN ESTER ENOLATES, 1, : REACTION OF THIOGLYCOLATE WITH ALDEHYDES USING DIALKYLBORYL TRIFLATE
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説明
With the assistance of the electron withdrawing effect of divalent sulfur substituent, boron ester enolates were formed from the corresponding oxygen esters in the presence of dialkylboryl trifluoromethanesulfonate. These novel oxygen ester enolates reacted smoothly with aldehydes to produce the usual syn-aldol products.
収録刊行物
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- Chemical & pharmaceutical bulletin
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Chemical & pharmaceutical bulletin 36 (11), 4619-4621, 1988-11-25
公益社団法人日本薬学会
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詳細情報 詳細情報について
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- CRID
- 1570572702505303168
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- NII論文ID
- 110003654736
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- NII書誌ID
- AA00602100
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- ISSN
- 00092363
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- 本文言語コード
- en
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- データソース種別
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- CiNii Articles