Formal [4+3] epoxide cascade reaction via a complementary ambiphilic pairing strategy.
about
S(N)Ar-based, facile synthesis of a library of benzothiaoxazepine-1,1'-dioxidesAn aldol-based build/couple/pair strategy for the synthesis of medium- and large-sized rings: discovery of macrocyclic histone deacetylase inhibitors.Automated synthesis of a 184-member library of thiadiazepan-1,1-dioxide-4-onesSynthesis of a stereochemically diverse library of medium-sized lactams and sultams via S(N)Ar cycloetherification.A formal [4 + 4] complementary ambiphile pairing reaction: a new cyclization pathway for ortho-quinone methidesSynthesis of amino-benzothiaoxazepine-1,1-dioxides utilizing a microwave-assisted, S(N)Ar protocolTowards the systematic exploration of chemical space.Chemistry of bridged lactams and related heterocyclesFacile (triazolyl)methylation of MACOS-derived benzofused sultams utilizing ROMP-derived OTP reagents.Exploring chemical diversity via a modular reaction pairing strategyExploration of cascade cyclizations terminated by tandem aromatic substitution: total synthesis of (+)-schweinfurthin A.Rapid, scalable assembly of stereochemically rich, mono- and bicyclic acyl sultamsScaling out by microwave-assisted, continuous flow organic synthesis (MACOS): multi-gram synthesis of bromo- and fluoro-benzofused sultams benzthiaoxazepine-1,1-dioxidesAccessing Stereochemically Rich Sultams via Microwave-Assisted, Continuous Flow Organic Synthesis (MACOS) Scale-out.Intramolecular monomer-on-monomer (MoM) Mitsunobu cyclization for the synthesis of benzofused thiadiazepine-dioxides.Synthesis of epoxybenzo[d]isothiazole 1,1-dioxides via a reductive-Heck, metathesis-sequestration protocolModular, One-Pot, Sequential Aziridine Ring Opening-S(N)Ar Strategy to 7-, 10-, and 11-Membered Benzo-Fused Sultams.Synthesis of an Isoindoline-Annulated, Tricyclic Sultam Library via Microwave-Assisted, Continuous-Flow Organic Synthesis (MACOS).Multicapillary Flow Reactor: Synthesis of 1,2,5-Thiadiazepane 1,1-Dioxide Library Utilizing One-Pot Elimination and Inter-/Intramolecular Double aza-Michael Addition Via Microwave-Assisted, Continuous-Flow Organic Synthesis (MACOS).Electrophilic aromatic prenylation via cascade cyclization.A conceptual framework for analysing and planning synthetic approaches to diverse lead-like scaffolds.A modular reaction pairing approach to the diversity-oriented synthesis of fused- and bridged-polycyclic sultams.Effective synthesis of chiral N-fluoroaryl aziridines through enantioselective aziridination of alkenes with fluoroaryl azides.Synthesis of stereochemically and skeletally diverse fused ring systems from functionalized C-glycosidesA modular lead-oriented synthesis of diverse piperazine, 1,4-diazepane and 1,5-diazocane scaffolds.
P2860
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P2860
Formal [4+3] epoxide cascade reaction via a complementary ambiphilic pairing strategy.
description
2010 nî lūn-bûn
@nan
2010 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի մարտին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Formal [4+3] epoxide cascade reaction via a complementary ambiphilic pairing strategy.
@ast
Formal [4+3] epoxide cascade reaction via a complementary ambiphilic pairing strategy.
@en
type
label
Formal [4+3] epoxide cascade reaction via a complementary ambiphilic pairing strategy.
@ast
Formal [4+3] epoxide cascade reaction via a complementary ambiphilic pairing strategy.
@en
prefLabel
Formal [4+3] epoxide cascade reaction via a complementary ambiphilic pairing strategy.
@ast
Formal [4+3] epoxide cascade reaction via a complementary ambiphilic pairing strategy.
@en
P2093
P2860
P356
P1433
P1476
Formal [4+3] epoxide cascade reaction via a complementary ambiphilic pairing strategy.
@en
P2093
Alan Rolfe
Paul R Hanson
Thiwanka B Samarakoon
P2860
P304
P356
10.1021/OL100035E
P407
P577
2010-03-01T00:00:00Z