Results 51 to 60 of about 337 (160)

Regio- and Diastereoselective [3 + 2]-Spiroannulation of Benzoxazines with Chalcones: A Rh(III)-Catalyzed Redox-Neutral Approach to α‑Aroyl Spiro-Indanamines

open access: yes
We report an atom-economic Rh­(III)-catalyzed [3 + 2]-spiroannulation reaction between cyclic ketimines and α,β-unsaturated carbonyl compounds, allowing the synthesis of novel spirocycles with concomitant generation of three stereogenic centers in one ...
Imtiaj Mondal (13039943)   +6 more
core   +2 more sources

Synergistic Sc(III)/Au(I)-Catalyzed Dearomative Spiroannulation of 2‑(Ethynyl)aryl Cyclopropanes with 2‑Aryl Indoles

open access: yes
The diastereoselective assembly of spiroindolenines via a synergistic scandium/gold-catalyzed dearomative spiroannulation is herein described. This protocol offers access to a wide variety of spiroindolenine derivatives in 86% average yield with moderate
Yanmin Huang (1515796)   +6 more
core   +1 more source

Synthetic approaches to komarovispiranes. Enantiospecific synthesis of bicyclo[3.3.0]octanespiro[3.1']cyclohexanes

open access: yes, 2007
A ring-closing metathesis based spiroannulation of cyclopentane and cyclohexanes at the C-3 carbon atom of a bicyclo[3.3.0]octane, as a model study directed towards the enantiospecific synthesis of the novel diterpenes komarovispiranes, is ...
Beeraiah, B., Srikrishna, A.
core   +2 more sources

2-(Trimethylsilyloxy)furan as a dianion equivalent: a two-step synthesis of functionalized spirocyclic butenolides.

open access: yes, 2006
[reaction: see text] The use of 2-(trimethylsilyloxy)furan derivatives as dianion equivalents leads to a general and connective spiroannulation protocol for the efficient preparation of spirocyclic ...
Maulide, Nuno   +3 more
core   +1 more source

2-(Trimethylsilyloxy)furan as a Dianion Equivalent:  A Two-Step Synthesis of Functionalized Spirocyclic Butenolides

open access: yes, 2016
The use of 2-(trimethylsilyloxy)furan derivatives as dianion equivalents leads to a general and connective spiroannulation protocol for the efficient preparation of spirocyclic ...
István E. Markó (2476828)   +1 more
core   +1 more source

Connective synthesis of spirovetivanes: Total synthesis of (+/-)-agarospirol, (+/-)-hinesol and (+/-)-alpha-vetispirene

open access: yes, 2004
A concise, connective synthesis of naturally occurring spirovetivanes 1 and 3, in racemic form, is presented. This novel approach involves the efficient assembly of the advanced intermediate 12 through a unique spiroannulation ...
Maulide, Nuno   +5 more
core   +1 more source

An Expedient Route to a Potent Gastrin/CCK-B Receptor Antagonist (+)-AG-041R

open access: yes, 2016
An enantiocontrolled synthesis of (+)-AG-041R (1), a potent gastrin/CCK-B receptor antagonist, has been achieved employing a chiral rhodium(II)-catalyzed, oxidative intramolecular aza-spiroannulation as the key ...
Yoshiharu Iwabuchi (1389561)   +3 more
core   +1 more source

A rapid access to spiroaminoketal framework.

open access: yes, 2005
A convergent and stereoselective synthesis of 1-oxa-7-azaspiro[5.5]undecane is described. This functional new spiroheterocycle is readily available from acetone ?n?-dimethylhydrazone via a double alkylation and subsequent spiroannulation ...
Sinibaldi, Marie-Eve   +4 more
core   +1 more source

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