about
Towards the optimal screening collection: a synthesis strategyA new paradigm for designing ring construction strategies for green organic synthesis: implications for the discovery of multicomponent reactions to build molecules containing a single ringRecent developments in antibacterial drug discovery: microbe-derived natural products--from collection to the clinic.Dioxindole in asymmetric catalytic synthesis: direct access to 3-substituted 3-hydroxy-2-oxindoles via 1,4-additions to nitroalkenes.A Reactivity-Driven Approach to the Discovery and Development of Gold-Catalyzed Organic Reactions.Constructing molecular complexity and diversity: total synthesis of natural products of biological and medicinal importance.A unified strategy for enantioselective total synthesis of cladiellin and briarellin diterpenes: total synthesis of briarellins E and F and the putative structure of alcyonin and revision of its structure assignment.Chemoselectivity: the mother of invention in total synthesis.Chemoenzymatic synthesis of the next generation of ultralow MW heparin therapeutics.Is there no end to the total syntheses of strychnine? Lessons learned in strategy and tactics in total synthesisDynamic foldamer chemistry.Enantioselective construction of spirooxindole derivatives through [3+2] annulation catalyzed by a bisthiourea as a multiple-hydrogen-bond donor.Highly efficient enantioselective construction of bispirooxindoles containing three stereocenters through an organocatalytic cascade Michael-cyclization reaction.Construction of bispirooxindoles containing three quaternary stereocentres in a cascade using a single multifunctional organocatalyst.Core-structure-motivated design of iminium-enolate organocascade reactions: enantioselective syntheses of 5,6-dihydroindolizines.Conjugate umpolung of β,β-disubstituted enals by dual catalysis with an N-heterocyclic carbene and a Brønsted acid: facile construction of contiguous quaternary stereocenters.Catalyst-controlled regio- and stereoselective synthesis of diverse 12H-6,12-methanodibenzo[d,g][1,3]dioxocines.YOU MAKE IT, I BREAK IT
P2860
Q28755381-9CD6D8DD-66AE-4F75-9E24-F643D81FB30EQ28817207-9E64F561-F6FB-46C3-85B2-E19BF884B2E2Q33234858-8E0F1F1C-90C5-4811-8D46-97C9B13BD999Q34256647-44F09586-E880-4116-9F26-3BF0959ABBCBQ34377834-A35C7605-F899-405B-813A-A2E53C8386FDQ36186718-7D999F80-F04A-4070-8173-644563E6BDC0Q37347081-45DD67FA-EBEA-4B79-AE32-9C78C3FDEC9AQ37395761-D71F3C29-7401-42C1-A1E6-240A8789DDC0Q37990946-FCCAB9E3-02C4-436D-A093-D02C3C8F3013Q37995122-A1E75671-BE72-46FC-9D49-D4DD4774302CQ38898016-8E3F1532-DB53-4367-B0AA-959286FBE1D3Q44183942-9EB96A11-CB70-4D2B-A5F7-9EC04AD57307Q45085125-BBE9FF99-BF10-47A5-9FF3-AAA2DD636CBAQ46008342-A633FDFD-0C3C-4310-AA10-EA47BE172411Q47870186-86DE8C7B-FB97-426D-AD6F-F46F6AE8C1BDQ51063034-202281A9-683C-417E-90A5-538891D300D8Q53547925-71FDF7C4-C64B-4E17-A538-20493060AF50Q57764036-4F44EE91-C74D-4E88-BD2D-C6CF48D3E539
P2860
description
2004 nî lūn-bûn
@nan
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
2004年论文
@zh
2004年论文
@zh-cn
name
The essence of total synthesis
@ast
The essence of total synthesis
@en
type
label
The essence of total synthesis
@ast
The essence of total synthesis
@en
prefLabel
The essence of total synthesis
@ast
The essence of total synthesis
@en
P2860
P356
P1476
The essence of total synthesis
@en
P2093
K C Nicolaou
Scott A Snyder
P2860
P304
11929-11936
P356
10.1073/PNAS.0403799101
P407
P577
2004-08-09T00:00:00Z