about
Contemporary Strategies for the Synthesis of Tetrahydropyran Derivatives: Application to Total Synthesis of Neopeltolide, a Marine Macrolide Natural ProductSynthesis of a 35-member stereoisomer library of bistramide A: evaluation of effects on actin state, cell cycle and tumor cell growth.Synthesis of reblastatin, autolytimycin, and non-benzoquinone analogues: potent inhibitors of heat shock protein 90.Total synthesis of (+)-isatisine A.Total synthesis of (+)-SCH 351448.Synthesis of isochromene-type scaffolds via single-flask Diels-Alder-[4 + 2]-annulation sequence of a silyl-substituted diene with menadione.Remote control of diastereoselectivity in intramolecular reactions of chiral allylsilanes.Pyrones to pyrans: enantioselective radical additions to acyloxy pyrones.Challenges in the synthesis of a unique mono-carboxylic acid antibiotic, (+)-zincophorin.De novo synthesis of natural products via the asymmetric hydration of polyenes.Impact of copper-catalyzed cross-coupling reactions in natural product synthesis: the emergence of new retrosynthetic paradigms.Design and synthesis of analogues of natural products.Barbier-type anti-Diastereo- and Enantioselective Synthesis of β-Trimethylsilyl, Fluorinated Methyl, Phenylthio Homoallylic Alcohols.De novo formal synthesis of (-)-apicularen A via an iterative asymmetric hydration sequence.Stereocontrolled synthesis of spirooxindoles through Lewis acid-promoted [5 + 2]-annulation of chiral silyl alcoholsAchmatowicz Reaction and its Application in the Syntheses of Bioactive Molecules.
P2860
Q26749672-E65B9D12-F3A4-42A7-8420-267AE8DF7D3BQ33405383-BCE883EF-CF90-4563-A6D6-38E34E9439A3Q33555574-8537E073-CC2F-4164-995B-5BD75FF9E8FFQ33781370-5FC29A1C-F339-4BC1-BA55-ECD963257A94Q33990694-BC239D60-B44F-4A58-81F9-0C50753400D7Q35185285-B69B9F5A-58A5-480D-A989-E9FA1981F37CQ36846623-1FD722E2-6BA8-498F-847D-B605316E03D3Q36865602-1132BF4E-5C55-4F16-8BB5-2E694FDE654BQ37566510-DDCCA369-05DB-48CC-AD03-B33EAC7C1229Q37874134-4AE61DCE-123B-4059-85C2-11BCDBB0152BQ38155074-35FFDC57-7E28-4D7A-9FDA-58E3BDA308C5Q38398596-FAB50122-F33C-4B9A-A3B5-82DECF6D5694Q40961509-23B8AF4A-E723-48BF-8C76-7DA1FE7C19B3Q42079148-C8763E01-C5C9-4A80-8A12-0030020781CDQ42583313-1B5FA799-EB00-4435-BE37-D96E20E541D2Q44167873-7B9A18F1-3C3F-4122-BD50-704505E9335B
P2860
description
2004 nî lūn-bûn
@nan
2004 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2004 թվականի մարտին հրատարակված գիտական հոդված
@hy
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
name
Total synthesis of (-)-apicularen A.
@ast
Total synthesis of (-)-apicularen A.
@en
type
label
Total synthesis of (-)-apicularen A.
@ast
Total synthesis of (-)-apicularen A.
@en
prefLabel
Total synthesis of (-)-apicularen A.
@ast
Total synthesis of (-)-apicularen A.
@en
P356
P1476
Total synthesis of (-)-apicularen A.
@en
P2093
James S Panek
P304
P356
10.1021/JA037957X
P407
P577
2004-03-01T00:00:00Z