Development of an Additive-Controlled, SmI2-mediated Stereoselective Sequence: Telescoped Spirocyclisation, Lactone Reduction and Peterson Elimination

Beilstein Journal of Organic Chemistry - Germany
doi 10.3762/bjoc.9.163
Full Text
Abstract

Available in full text

Date
Authors
Publisher

Beilstein Institut

Related search

Highly Stereoselective Construction of Spiro[4.5]decanes by SmI2-Promoted Ketyl Radical Mediated Tandem Cyclization

English

Stereoselective Synthesis of Enamides by a Peterson Reaction Manifold

Organic Letters
BiochemistryOrganic ChemistryTheoretical ChemistryPhysical
2001English

Additive-Controlled Stereoselective Glycosylations of Oxazolidinone-Protected Glucosamine and Galactosamine Thioglycoside Donors Based on Preactivation Protocol

Synlett
Organic Chemistry
2010English

A Fully-Telescoped, Aqueous, Auxiliary-Mediated Asymmetric Transformation

Arkivoc
Organic Chemistry
2005English

Development of a Stereoselective Co-Mediated Dihydropyran Ring Contraction

English

Controlled Induction and Targeted Elimination of P16ink4a-High Chondrocytes to Investigate Senescence-Mediated Cartilage Dysfunction

Osteoarthritis and Cartilage
Sports MedicineRheumatologyOrthopedicsBiomedical Engineering
2019English

Elimination or Reduction of Diseases?

Journal of Epidemiology and Community Health
EpidemiologyPublic HealthOccupational HealthEnvironmental
1989English

Inhaled Corticosteroid Reduction and Elimination in Patients With Persistent Asthma Receiving SalmeterolA Randomized Controlled Trial

JAMA - Journal of the American Medical Association
Medicine
2001English

One-Pot L -Proline-Mediated Stereoselective Α-C(sp2 )-H Fluorination of Α,β-Unsaturated Aldehydes Through Methoxyfluorination-Elimination

European Journal of Organic Chemistry
Organic ChemistryTheoretical ChemistryPhysical
2018English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy