مشارك في 6 تفاعل

1130863

CC[C@H](NC(=O)OCc1ccccc1)C(O[Si](C)(C)C(C)(C)C)C1(C(=O)OC(C)(C)C)CC1
Reaction #1260794
title compound
المردود 98.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_11
CCOC(=O)CC(O[Si](C)(C)C(C)(C)C)[C@H](CC)NC(=O)OCc1ccccc1
Reaction #1260801
ethyl(4S)-4-{[(benzyloxy)carbonyl]amino}-3-(tert-butyldimethylsilyloxy)hexanoate
المردود 74.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_11
CC[C@H](NC(=O)OCc1ccccc1)C(O[Si](C)(C)C(C)(C)C)C1(C(=O)OC(C)(C)C)CC1
Reaction #2054468
title compound
المردود 98.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_04
CCOC(=O)CC(O[Si](C)(C)C(C)(C)C)[C@H](CC)NC(=O)OCc1ccccc1
Reaction #2054474
ethyl (4S)-4-{[(benzyloxy)carbonyl]amino}-3-(tert-butyldimethylsilyloxy)hexanoate
المردود 74.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_04
CC(C)[C@H]1[C@@H](O[Si](C)(C)C(C)(C)C)CCN1C(=O)OCc1ccccc1
Reaction #2133839
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_11
C=CCC(O[Si](C)(C)C(C)(C)C)[C@H](C)NC(=O)OCc1ccccc1
Reaction #2133841
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_11