DMAP

CC(C)(C)[Si](C)(C)Oc1cc2ccc(Br)cc2cc1C12CC3CC(CC(C3)C1)C2
Reaction #1239
7-(1-adamantyl)-6-tert-butyldimethylsilyloxy-2-bromonaphthalene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)c1ccc(I)nc1
Reaction #1321
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCC1=Cc2c(cccc2-c2ccccc2)C1
Reaction #1354
desired product
المردود 73.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)CC1=Cc2c(cccc2-c2cccc3ccccc23)C1
Reaction #1361
desired product
المردود 93.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(c1ccc(OCCN2CCCCC2)cc1)c1c(-c2ccc(O)cc2)sc2cc(O)ccc12
Reaction #1586
Raloxifene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)C(=O)Nc1ncnc2c1ncn2[C@H]1CC=CO1
Reaction #1654
(R)-N-[9-(2,3-Dihydro-2-furanyl)-9H-purin-6-yl]-2,2-dimethylpropanamide
المردود 94.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCCCc1cc2c(cc1C(=O)Oc1ccc(C(=O)OCc3ccccc3)cn1)C(C)(C)CCC2(C)C
Reaction #1729
benzyl 6-(3-hexyl-5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-naphthalen-2-yl-carbonyloxy)-nicotinate
المردود 57.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C[Si](C)(C)C/C=C/COC(=O)c1ccc(O)nc1
Reaction #1735
4-trimethylsilanyl-(E)-but-2-enyl 6-hydroxy-nicotinate
المردود 38.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(=O)OC1CCC(c2ccccc2)CC1
Reaction #1745
O-acetyl-4-phenylcyclohexanol
المردود 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C=CCC(=O)CNC(=O)OCC1c2ccccc2-c2ccccc21
Reaction #1845
Fmoc-Gly-Allyl
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)OC(=O)N[C@H](Cc1c[nH]c2ccccc12)C(=O)OCc1ccccc1
Reaction #2002
N-(t-Butoxycarbonyl)-D-tryptophan benzyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C=CCOC(=O)[C@@H](CCc1ccccc1)NC(=O)OC(C)(C)C
Reaction #2009
N-(t-Butoxycarbonyl)-D-homophenylalanine allyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C=CCOC(=O)[C@@H](COCc1ccccc1)NC(=O)OC(C)(C)C
Reaction #2018
N-(t-Butoxycarbonyl)-O-Benzyl-D-Serine Allyl Ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(=O)NC(CC(=O)OCc1ccccc1)C(C)=O
Reaction #2260
title compound
المردود 82.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1ccc(C(CC(N)=O)N2C(=O)c3ccccc3C2=O)cc1OC1CCCC1
Reaction #2444
product
المردود 62.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1ccccc1NS(=O)(=O)c1ccc(C)cc1
Reaction #2503
title compound
المردود 62.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)[Si](C)(C)OC1C=CC(=O)C1
Reaction #2634
title compound
المردود 83.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCC(=O)Nc1ccc(C(=O)N2CCOCC2)cc1OCc1ccc(-c2ccccc2-c2nnnn2C(c2ccccc2)(c2ccccc2)c2ccccc2)cc1
Reaction #2826
3-[[2'-(1-triphenylmethyltetrazol-5-yl)biphenyl-4-yl]methyloxy]-4-valeramidobenzoic acid morpholide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(=O)NCC(CC(Cc1cc(C(F)(F)F)cc(C(F)(F)F)c1)N1CCC(NC(C)=O)(c2ccccc2)CC1)c1ccc(Cl)c(Cl)c1
Reaction #3139
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CN(C)CCNc1nc2cc(OC(=O)C(C)(C)C)ccc2c2c1C(=O)c1ccccc1-2
Reaction #3253
title compound
المردود 83.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
الصفحة 1التالي