Triflimide (HNTf2)–catalyzed aldehyde cross-aldol reaction using “super silyl” enol ethers

Matthew B Boxer; Hisashi Yamamoto

doi:10.1038/nprot.2006.389

Triflimide (HNTf2)–catalyzed aldehyde cross-aldol reaction using “super silyl” enol ethers

Nature Protocols ◽

10.1038/nprot.2006.389 ◽

2006 ◽

Vol 1 (5) ◽

pp. 2434-2438 ◽

Cited By ~ 22

Author(s):

Matthew B Boxer ◽

Hisashi Yamamoto

Keyword(s):

Aldol Reaction ◽

Enol Ethers ◽

Silyl Enol Ethers ◽

Super Silyl

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ChemInform Abstract: Enantioselective and Diastereoselective Catalysis of the Mukaiyama Aldol Reaction: Ene Mechanism in Titanium-Catalyzed Aldol Reactions of Silyl Enol Ethers.

ChemInform ◽

10.1002/chin.199349056 ◽

2010 ◽

Vol 24 (49) ◽

pp. no-no

Author(s):

K. MIKAMI ◽

S. MATSUKAWA

Keyword(s):

Aldol Reaction ◽

Aldol Reactions ◽

Enol Ethers ◽

Silyl Enol Ethers ◽

Mukaiyama Aldol Reaction ◽

Mukaiyama Aldol

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ChemInform Abstract: Trityl Salt-Catalyzed Aldol Reaction Between α,β-Acetylenic Ketones and Silyl Enol Ethers.

ChemInform ◽

10.1002/chin.198920227 ◽

1989 ◽

Vol 20 (20) ◽

Author(s):

S. KOBAYASHI ◽

S. MATSUI ◽

T. MUKAIYAMA

Keyword(s):

Aldol Reaction ◽

Enol Ethers ◽

Silyl Enol Ethers

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The Aldol Reaction of Silyl Enol Ethers with Aldehydes in Aqueous Media

Tetrahedron Letters ◽

10.1016/s0040-4039(00)91691-5 ◽

1992 ◽

Vol 33 (12) ◽

pp. 1625-1628 ◽

Cited By ~ 107

Author(s):

Shū Kobayashi ◽

Iwao Hachiya

Keyword(s):

Aldol Reaction ◽

Aqueous Media ◽

Enol Ethers ◽

Silyl Enol Ethers

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ChemInform Abstract: N-Triflylthiophosphoramide Catalyzed Enantioselective Mukaiyama Aldol Reaction of Aldehydes with Silyl Enol Ethers of Ketones.

ChemInform ◽

10.1002/chin.201043064 ◽

2010 ◽

Vol 41 (43) ◽

pp. no-no

Author(s):

Cheol Hong Cheon ◽

Hisashi Yamamoto

Keyword(s):

Aldol Reaction ◽

Enol Ethers ◽

Silyl Enol Ethers ◽

Mukaiyama Aldol Reaction ◽

Mukaiyama Aldol

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ChemInform Abstract: Catalytic Asymmetric Aldol Reaction of Silyl Enol Ethers with Aldehydes by the Use of Chiral Diamine-Coordinated Tin(II) Triflate.

ChemInform ◽

10.1002/chin.199037101 ◽

1990 ◽

Vol 21 (37) ◽

Author(s):

T. MUKAIYAMA ◽

S. KOBAYASHI ◽

H. UCHIRO ◽

I. SHIINA

Keyword(s):

Aldol Reaction ◽

Asymmetric Aldol ◽

Enol Ethers ◽

Silyl Enol Ethers ◽

Chiral Diamine ◽

Asymmetric Aldol Reaction ◽

Catalytic Asymmetric

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Aromatic aldehyde-selective aldol addition with aldehyde-derived silyl enol ethers

Chemical Communications ◽

10.1039/c7cc08936h ◽

2018 ◽

Vol 54 (4) ◽

pp. 374-377 ◽

Cited By ~ 4

Author(s):

Takahiro Kawajiri ◽

Reiya Ohta ◽

Hiromichi Fujioka ◽

Hironao Sajiki ◽

Yoshinari Sawama

Keyword(s):

Aromatic Aldehyde ◽

Aldol Reaction ◽

Aliphatic Aldehydes ◽

Enol Ethers ◽

Silyl Enol Ethers ◽

Mukaiyama Aldol Reaction ◽

Mukaiyama Aldol ◽

Aldol Addition

Unprecedented chemoselectivity between aromatic and aliphatic aldehydes has been achieved in the Mukaiyama aldol reaction using aldehyde-derived silyl enol ethers.

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ChemInform Abstract: Surface-Mediated Solid Phase Reaction. Part 5. Aldol Reaction of Silyl Enol Ethers with Aldehydes on a Solid Surface of Neutral Alumina: Selectivity for anti Aldols.

ChemInform ◽

10.1002/chin.199343068 ◽

2010 ◽

Vol 24 (43) ◽

pp. no-no

Author(s):

B. C. RANU ◽

R. CHAKRABORTY

Keyword(s):

Solid Surface ◽

Solid Phase ◽

Aldol Reaction ◽

Solid Phase Reaction ◽

Phase Reaction ◽

Neutral Alumina ◽

Enol Ethers ◽

Silyl Enol Ethers

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Dicobalt hexacarbonyl-complex of propynals in organic synthesis: -selective aldol reaction of cobalt-complexed propynals with silyl enol ethers

Tetrahedron Letters ◽

10.1016/s0040-4039(01)93815-8 ◽

1989 ◽

Vol 30 (41) ◽

pp. 5623-5626 ◽

Cited By ~ 20

Author(s):

Chisato Mukai ◽

Kazuyoshi Nagami ◽

Miyoji Hanaoka

Keyword(s):

Organic Synthesis ◽

Aldol Reaction ◽

Enol Ethers ◽

Silyl Enol Ethers ◽

Dicobalt Hexacarbonyl

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ChemInform Abstract: Asymmetric Aldol Reaction Between Achiral Silyl Enol Ethers and Achiral Aldehydes by Use of a Chiral, Promoter System.

ChemInform ◽

10.1002/chin.199136084 ◽

2010 ◽

Vol 22 (36) ◽

pp. no-no

Author(s):

S. KOBAYASHI ◽

H. UCHIRO ◽

Y. FUJISHITA ◽

I. SHIINA ◽

T. MUKAIYAMA

Keyword(s):

Aldol Reaction ◽

Asymmetric Aldol ◽

Enol Ethers ◽

Silyl Enol Ethers ◽

Asymmetric Aldol Reaction ◽

Promoter System

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Lanthanide Triflates as Water-Tolerant Lewis Acids. Activation of Commercial Formaldehyde Solution and Use in the Aldol Reaction of Silyl Enol Ethers with Aldehydes in Aqueous Media

The Journal of Organic Chemistry ◽

10.1021/jo00092a017 ◽

1994 ◽

Vol 59 (13) ◽

pp. 3590-3596 ◽

Cited By ~ 280

Author(s):

Shu Kobayashi ◽

Iwao Hachiya

Keyword(s):

Lewis Acids ◽

Aldol Reaction ◽

Aqueous Media ◽

Formaldehyde Solution ◽

Enol Ethers ◽

Silyl Enol Ethers

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