Diastereoselectivity in the osmium-catalyzed dihydroxylation of allylic amides and carbamates

DOI: 10.1016/0957-4166(94)80024-3

Source and publish data:

Tetrahedron Asymmetry p. 625 - 632 (1994)

Update date:2022-08-04

Topics:

Authors:

Krysan Krysan

Rockway Rockway

Haight Haight

Read Full Text PDF DownLoad Join now for total 90,000,000 free articles

Article abstract of DOI:10.1016/0957-4166(94)80024-3

The stereochemistry of the osmium-catalyzed dihydroxylation of a series of chiral allylic amides and carbamates has been studied. The diastereoselectivity of these reactions was found to be dependent upon the solvent and the nitrogen protecting group as w

Full text of DOI:10.1016/0957-4166(94)80024-3

Products guided by the article

Product name:N-((Z)-(S)-1-Cyclohexylmethyl-5-methyl-hex-2-enyl)-acetamide

Cas No:156540-59-9

R&D Labs maybe for 156540-59-9

Anhui Eapearl Chemical Co., Ltd.

Contact:86-562-5858458

Address:358 South Huaihe Road
Dalian Synco Chemical Co., Ltd.

Contact:+86-411-83635150

Address:Rm 1004, 24, Tangshan Street, Dalian
Synchemie Co., Ltd.

website:http://www.synchemie.com/

Contact:+86-574-87642758

Address:Room 901, Yinyi Bund Building， 132 Renmin Road
Wuhan Fortuna Chemical Co.,Ltd

website:http://www.fortunachem.com

Contact:86-27-59207850

Address:Add: Room 2015, No.2 Building, Kaixin Mansion No.107 Jinqiao Avenue, Wuhan, China
Changzhou Anyi Biochem Co., Ltd.(expird)

Contact:+86-519-88836158

Address:no,51 caoda

Relevant to this article

Enantioselective synthesis of enol lactones from tandem Michael addition/lactonization catalyzed by a chiral squaramide catalyst

Doi:10.1016/j.tetasy.2014.01.005
(2014)
Remarkable regioisomer control in the hydrogel formation from a two-component mixture of pyridine-end oligo(p-phenylenevinylene)s and N-decanoyl-l-alanine

Doi:10.1002/chem.201302100
(2013)
Doi:10.1039/j39680002016
(1968)
Structural study-guided development of versatile phase-transfer catalysts for asymmetric conjugate additions of cyanide

Doi:10.1002/anie.201105536
(2011)
Imidazolium-based organoiridium-functionalized periodic mesoporous organosilica boosts enantioselective reduction of α-cyanoacetophenones, α-nitroacetophenones, and β-ketoesters

Doi:10.1016/j.jcat.2014.09.019
(2014)
Janus-type organopotassium chemistry observed in deprotonation of mesoionic imidazolium aminides and amino N-heterocyclic carbenes: Coordination and organometallic polymers

Doi:10.1039/c3cc49517e
(2014)

Article Doi