An Efficient Molybdenum(VI)-Catalyzed Direct Substitution of Allylic Alcohols with Nitrogen, Oxygen, and Carbon Nucleophiles

Hongwei Yang; Ling Fang; Ming Zhang; Chengjian Zhu

doi:10.1002/ejoc.200800976

An Efficient Molybdenum(VI)-Catalyzed Direct Substitution of Allylic Alcohols with Nitrogen, Oxygen, and Carbon Nucleophiles

European Journal of Organic Chemistry ◽

10.1002/ejoc.200800976 ◽

2009 ◽

Vol 2009 (5) ◽

pp. 666-672 ◽

Cited By ~ 62

Author(s):

Hongwei Yang ◽

Ling Fang ◽

Ming Zhang ◽

Chengjian Zhu

Keyword(s):

Allylic Alcohols ◽

Carbon Nucleophiles ◽

Direct Substitution

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ChemInform Abstract: Fluorinated Alcohols as Promoters for the Metal-Free Direct Substitution Reaction of Allylic Alcohols with Nitrogenated, Silylated, and Carbon Nucleophiles.

ChemInform ◽

10.1002/chin.201252026 ◽

2012 ◽

Vol 43 (52) ◽

pp. no-no

Author(s):

Paz Trillo ◽

Alejandro Baeza ◽

Carmen Najera

Keyword(s):

Substitution Reaction ◽

Allylic Alcohols ◽

Metal Free ◽

Carbon Nucleophiles ◽

Fluorinated Alcohols ◽

Direct Substitution

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Fluorinated Alcohols As Promoters for the Metal-Free Direct Substitution Reaction of Allylic Alcohols with Nitrogenated, Silylated, and Carbon Nucleophiles

The Journal of Organic Chemistry ◽

10.1021/jo301049w ◽

2012 ◽

Vol 77 (17) ◽

pp. 7344-7354 ◽

Cited By ~ 87

Author(s):

Paz Trillo ◽

Alejandro Baeza ◽

Carmen Nájera

Keyword(s):

Substitution Reaction ◽

Allylic Alcohols ◽

Metal Free ◽

Carbon Nucleophiles ◽

Fluorinated Alcohols ◽

Direct Substitution

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ChemInform Abstract: An Efficient Molybdenum(VI)-Catalyzed Direct Substitution of Allylic Alcohols with Nitrogen, Oxygen, and Carbon Nucleophiles.

ChemInform ◽

10.1002/chin.200923095 ◽

2009 ◽

Vol 40 (23) ◽

Author(s):

Hongwei Yang ◽

Ling Fang ◽

Ming Zhang ◽

Chengjian Zhu

Keyword(s):

Allylic Alcohols ◽

Carbon Nucleophiles ◽

Direct Substitution

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Direct substitution of secondary allylic alcohols with O-silylated ketene acetals in 3.0 M lithium perchlorate-diethyl ether - An alternative to the [1,3] sigmatropic rearrangement of allyl vinyl ethers

Tetrahedron Letters ◽

10.1016/s0040-4039(00)61272-8 ◽

1992 ◽

Vol 33 (33) ◽

pp. 4735-4738 ◽

Cited By ~ 25

Author(s):

Paul A. Grieco ◽

Jon L. Collins ◽

Kenneth J. Henry

Keyword(s):

Diethyl Ether ◽

Lithium Perchlorate ◽

Sigmatropic Rearrangement ◽

Allylic Alcohols ◽

Vinyl Ethers ◽

Direct Substitution ◽

Ketene Acetals ◽

Allyl Vinyl Ethers

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ChemInform Abstract: Direct Substitution of Secondary Allylic Alcohols with O-Silylated Ketene acetals in 3.0 M Lithium Perchlorate-Diethyl Ether. An Alternative to the (1.3)Sigmatropic Rearrangement of Allyl Vinyl Ethers.

ChemInform ◽

10.1002/chin.199301150 ◽

2010 ◽

Vol 24 (1) ◽

pp. no-no

Author(s):

P. A. GRIECO ◽

J. L. COLLINS ◽

K. J. JUN. HENRY

Keyword(s):

Diethyl Ether ◽

Lithium Perchlorate ◽

Sigmatropic Rearrangement ◽

Allylic Alcohols ◽

Vinyl Ethers ◽

Direct Substitution ◽

Ketene Acetals ◽

Allyl Vinyl Ethers

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ChemInform Abstract: Direct Substitution of 2-Benzenesulfonylpiperidines and -pyrrolidines by Carbon Nucleophiles: Synthesis of the Pyrrolidine Alkaloid Ruspolinone.

ChemInform ◽

10.1002/chin.199022279 ◽

1990 ◽

Vol 21 (22) ◽

Author(s):

D. S. BROWN ◽

T. HANSSON ◽

S. V. LEY

Keyword(s):

Carbon Nucleophiles ◽

Direct Substitution

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Direct substitution of propargylic alcohol with oxygen, nitrogen, and carbon nucleophiles catalyzed by molybdenum(VI)

Tetrahedron Letters ◽

10.1016/j.tetlet.2009.12.128 ◽

2010 ◽

Vol 51 (8) ◽

pp. 1176-1179 ◽

Cited By ~ 22

Author(s):

Ming Zhang ◽

Hongwei Yang ◽

Yixiang Cheng ◽

Yuhua Zhu ◽

Chengjian Zhu

Keyword(s):

Carbon Nucleophiles ◽

Propargylic Alcohol ◽

Direct Substitution

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Direct Substitution of 2-Benzenesulphonylpiperidines and -pyrrolidines by Carbon Nucleophiles: Synthesis of the Pyrrolidine Alkaloid Ruspolinone

Synlett ◽

10.1055/s-1990-20983 ◽

1990 ◽

Vol 1990 (01) ◽

pp. 48-49 ◽

Cited By ~ 21

Author(s):

Dearg S. Brown ◽

Thomas Hansson ◽

Steven V. Ley

Keyword(s):

Carbon Nucleophiles ◽

Direct Substitution

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Aerobic Oxidative Coupling between Carbon Nucleophiles and Allylic Alcohols: A Strategy to Construct β-(Hetero)Aryl Ketones and Aldehydes through Hydrogen Migration

Chemistry - A European Journal ◽

10.1002/chem.201302962 ◽

2013 ◽

Vol 19 (46) ◽

pp. 15462-15466 ◽

Cited By ~ 26

Author(s):

Liangbin Huang ◽

Ji Qi ◽

Xia Wu ◽

Wanqing Wu ◽

Huanfeng Jiang

Keyword(s):

Oxidative Coupling ◽

Allylic Alcohols ◽

Hydrogen Migration ◽

Carbon Nucleophiles ◽

Aryl Ketones

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ChemInform Abstract: Aerobic Oxidative Coupling Between Carbon Nucleophiles and Allylic Alcohols: A Strategy to Construct β-(Hetero)aryl Ketones and Aldehydes Through Hydrogen Migration.

ChemInform ◽

10.1002/chin.201418111 ◽

2014 ◽

Vol 45 (18) ◽

pp. no-no

Author(s):

Liangbin Huang ◽

Ji Qi ◽

Xia Wu ◽

Wanqing Wu ◽

Huanfeng Jiang

Keyword(s):

Oxidative Coupling ◽

Allylic Alcohols ◽

Hydrogen Migration ◽

Carbon Nucleophiles ◽

Aryl Ketones

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