about
Efficient synthesis of the C(7)-C(20) subunit of amphidinolides C and FEnantioselective total synthesis of amphidinolide F.Highly Selective Synthesis of Halomon, Plocamenone, and Isoplocamenone.Total synthesis of cytotoxic macrolide amphidinolide B1 and the proposed structure of amphidinolide B2.Amphidinolide B: total synthesis, structural investigation, and biological evaluation.Exploiting hidden symmetry in natural products: total syntheses of amphidinolides C and F.Direct Conversion of Aldehydes and Ketones to Allylic Halides by a NbX(5-)[3,3] RearrangementAllylic and allenic halide synthesis via NbCl(5)- and NbBr(5)-mediated alkoxide rearrangements.Recent developments of direct rhenium-catalyzed [1,3]-transpositions of allylic alcohols and their silyl ethers.Total syntheses of the archazolids: an emerging class of novel anticancer drugs.Synthesis and activity of the archazolid western hemisphere.Application of tandem ring-closing enyne metathesis: formal total synthesis of (-)-cochleamycin A.Synthesis of recyclable fluorous chiral ligands and evaluation of their catalytic activity toward asymmetric addition of dimethylzinc to aldehydes.
P2860
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P2860
description
2006 nî lūn-bûn
@nan
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
2006年论文
@zh
2006年论文
@zh-cn
name
Synthetic studies on amphidinolide B1.
@en
type
label
Synthetic studies on amphidinolide B1.
@en
prefLabel
Synthetic studies on amphidinolide B1.
@en
P2093
P2860
P356
P1433
P1476
Synthetic studies on amphidinolide B1.
@en
P2093
Amit K Mandal
Craig M Crews
John S Schneekloth
Kouji Kuramochi
P2860
P304
P356
10.1021/OL052620G
P407
P577
2006-02-01T00:00:00Z