Dual control of selectivity in the synthesis of homochiral densely substituted cyclopropanes via the addition of nucleophiles to in situ generated cyclopropenes

被引：0

作者：

Ryabchuk, Pavel ^{[1
]}

Edwards, Andrew ^{[1
]}

Babkov, Ivan ^{[1
]}

Matheny, Jonathon ^{[1
]}

Rubina, Marina ^{[1
]}

Rubin, Michael ^{[1
]}

机构：

[1] Univ Kansas, Dept Chem, Lawrence, KS 66045 USA

来源：

ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY | 2013年 / 245卷

关键词：

D O I：

暂无

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

511-ORGN

引用

页数：1

共 39 条

[1] Dual control of selectivity in the synthesis of donor-acceptor cyclopropanes via the addition of oxygen and nitrogen based nucleophiles to in situ generated cyclopropenes
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[7] CYCLOPENTANE SYNTHESIS VIA FREE RADICAL-MEDIATED ADDITION OF FUNCTIONALIZED ALKENES TO SUBSTITUTED VINYL CYCLOPROPANES
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[8] ASYMMETRIC-SYNTHESIS OF ALPHA-SUBSTITUTED BENZYL ALCOHOLS VIA THE STEREOSELECTIVE ADDITION OF NUCLEOPHILES TO HOMOCHIRAL TRICARBONYL(ETA-6-O-TRIALKYLSILYLBENZALDEHYDE)CHROMIUM(O) COMPLEXES
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[9] Cu-Catalyzed one-pot synthesis of thiochromeno-quinolinone and thiochromeno-thioflavone via oxidative double hetero Michael addition using in situ generated nucleophiles
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[J]. CHEMICAL COMMUNICATIONS, 2020, 56 (62) : 8826 - 8829
[10] Stereoselective Synthesis of Thiochromenes via Intramolecular Tandem Thio-Michael Addition of in Situ Generated α,β-Unsaturated Aldehydes
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[J]. JOURNAL OF ORGANIC CHEMISTRY, 2014, 79 (07): : 3111 - 3118

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