µ-Oxo-bis(chlorotriphenylbismuth): a mild reagent for the oxidation of the hydroxy group, especially in allylic alcohols

Journal of the Chemical Society Chemical Communications ◽

10.1039/c39780001099 ◽

1978 ◽

pp. 1099-1100 ◽

Cited By ~ 28

Author(s):

Derek H. R. Barton ◽

Jonathan P. Kitchin ◽

William B. Motherwell

Keyword(s):

Hydroxy Group ◽

Allylic Alcohols

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Hydroxy-Group Directivity in the Nitroso Ene Reaction: Diastereo- and Regioselective Amination of Chiral Allylic Alcohols

Journal of the American Chemical Society ◽

10.1021/ja001752w ◽

2000 ◽

Vol 122 (40) ◽

pp. 9846-9847 ◽

Cited By ~ 14

Author(s):

Waldemar Adam ◽

Nils Bottke

Keyword(s):

Hydroxy Group ◽

Allylic Alcohols ◽

Ene Reaction

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ChemInform Abstract: μ-OXO-BIS(CHLOROTRIPHENYLBISMUTH): A MILD REAGENT FOR THE OXIDATION OF THE HYDROXY GROUP, ESPECIALLY IN ALLYLIC ALCOHOLS

Chemischer Informationsdienst ◽

10.1002/chin.197917159 ◽

1979 ◽

Vol 10 (17) ◽

Author(s):

D. H. R. BARTON ◽

J. P. KITCHIN ◽

W. B. MOTHERWELL

Keyword(s):

Hydroxy Group ◽

Allylic Alcohols

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A Highly Chemoselective, Diastereoselective, and Regioselective Epoxidation of Chiral Allylic Alcohols with Hydrogen Peroxide, Catalyzed by Sandwich-Type Polyoxometalates: Enhancement of Reactivity and Control of Selectivity by the Hydroxy Group through Metal−Alcoholate Bonding

The Journal of Organic Chemistry ◽

10.1021/jo0266386 ◽

2003 ◽

Vol 68 (5) ◽

pp. 1721-1728 ◽

Cited By ~ 80

Author(s):

Waldemar Adam ◽

Paul L. Alsters ◽

Ronny Neumann ◽

Chantu R. Saha-Möller ◽

Dorit Sloboda-Rozner ◽

...

Keyword(s):

Hydrogen Peroxide ◽

Hydroxy Group ◽

Allylic Alcohols ◽

Sandwich Type ◽

And Control ◽

Sandwich Type Polyoxometalates

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A Highly Chemoselective, Diastereoselective, and Regioselective Epoxidation of Chiral Allylic Alcohols with Hydrogen Peroxide, Catalyzed by Sandwich-Type Polyoxometalates: Enhancement of Reactivity and Control of Selectivity by the Hydroxy Group Through Metal—Alcoholate Bonding.

ChemInform ◽

10.1002/chin.200327042 ◽

2003 ◽

Vol 34 (27) ◽

Author(s):

Waldemar Adam ◽

Paul L. Alsters ◽

Ronny Neumann ◽

Chantu R. Saha-Moeller ◽

Dorit Sloboda-Rozner ◽

...

Keyword(s):

Hydrogen Peroxide ◽

Hydroxy Group ◽

Allylic Alcohols ◽

Sandwich Type ◽

And Control ◽

Sandwich Type Polyoxometalates

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ChemInform Abstract: Reduction of α,β-Unsaturated Ketones and the Respective Allylic Alcohols, Bearing a Phenylsulfonyl or Phenylsulfanyl Group in the α Position. Hydroxy Group Controlled Stereoselective Reduction of 3α- and 3β-Hydroxy-4-(phenylsulfonyl)c

ChemInform ◽

10.1002/chin.200039170 ◽

2000 ◽

Vol 31 (39) ◽

pp. no-no

Author(s):

Karol Michalak ◽

Wiaczeslaw Stepanenko ◽

Jerzy Wicha

Keyword(s):

Hydroxy Group ◽

Allylic Alcohols ◽

Stereoselective Reduction ◽

Unsaturated Ketones

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ChemInform Abstract: Hydroxy-Group Directivity in the Nitroso Ene Reaction: Diastereo- and Regioselective Amination of Chiral Allylic Alcohols.

ChemInform ◽

10.1002/chin.200103032 ◽

2001 ◽

Vol 32 (3) ◽

pp. no-no

Author(s):

Waldemar Adam ◽

Nils Bottke

Keyword(s):

Hydroxy Group ◽

Allylic Alcohols ◽

Ene Reaction

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Regio- and Diastereoselective Catalytic Epoxidation of Chiral Allylic Alcohols with Hexafluoroacetone Perhydrate. Hydroxy-Group Directivity through Hydrogen Bonding

The Journal of Organic Chemistry ◽

10.1021/jo982025a ◽

1999 ◽

Vol 64 (4) ◽

pp. 1274-1277 ◽

Cited By ~ 14

Author(s):

Waldemar Adam ◽

Hans-Georg Degen ◽

Chantu R. Saha-Möller

Keyword(s):

Hydrogen Bonding ◽

Hydroxy Group ◽

Allylic Alcohols ◽

Catalytic Epoxidation

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ChemInform Abstract: Hydroxy Group Directivity in the Epoxidation of Chiral Allylic Alcohols: Control of Diastereoselectivity Through Allylic Strain and Hydrogen Bonding

ChemInform ◽

10.1002/chin.199942298 ◽

2010 ◽

Vol 30 (42) ◽

pp. no-no

Author(s):

Waldemar Adam ◽

Thomas Wirth

Keyword(s):

Hydrogen Bonding ◽

Hydroxy Group ◽

Allylic Alcohols

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Ene Reaction of Singlet Oxygen, Triazolinedione, and Nitrosoarene with Chiral Deuterium-Labeled Allylic Alcohols: The Interdependence of Diastereoselectivity and Regioselectivity Discloses Mechanistic Insights into the Hydroxy-Group Directivity

Journal of the American Chemical Society ◽

10.1021/ja027800p ◽

2002 ◽

Vol 124 (48) ◽

pp. 14403-14409 ◽

Cited By ~ 16

Author(s):

Waldemar Adam ◽

Nils Bottke ◽

Oliver Krebs ◽

Ioannis Lykakis ◽

Michael Orfanopoulos ◽

...

Keyword(s):

Singlet Oxygen ◽

Hydroxy Group ◽

Allylic Alcohols ◽

Ene Reaction

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On reduction of α,β-unstaurated ketones and the respective allylic alcohols, bearing a phenylsulfonyl or phenylsulfanyl group in the α position. Hydroxy group-controlled stereoselective reduction of 3α- and 3β-hydroxy-4-(phenylsulfonyl)cholest-4-ene

Journal of the Chemical Society Perkin Transactions 1 ◽

10.1039/b000600i ◽

2000 ◽

pp. 1587-1594 ◽

Cited By ~ 3

Author(s):

Karol Michalak ◽

Wiaczesław Stepanenko ◽

Jerzy Wicha

Keyword(s):

Hydroxy Group ◽

Allylic Alcohols ◽

Stereoselective Reduction

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