Synthesis of the ABH rings of ecteinascidin 597 using a connective Pummerer-type cyclisation
A connective Pummerer-type cyclisation involving a cysteine derivative and an N-benzyl glyoxamide 3 has been applied in an asymmetric synthesis of the protected ABH rings 2 of the antitumour and antimicrobial natural product ecteinascidin 597.
Smith, Laura H. S.,Nguyen, Trung Thanh,Sneddon, Helen F.,Procter, David J.
p. 10821 - 10823
(2011/11/05)
More Articles about upstream products of 1339231-97-8
Get Best Price for1339231-97-82,2,2-trichloroethyl ((1R,4R,8R)-9,10,12-trimethoxy-13-(4-methoxybenzyl)-11-methyl-5,14-dioxo-1,3,4,5,7,8-hexahydro-8,1-(epiminomethano)benzo[g][1,5]oxathiecin-4-yl)carbamate