L-arabinose

O=C[C@H](O)[C@@H](O)[C@H](O)CO
Reaction #362832
D-xylose
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
NN=C[C@H](O)[C@@H](O)[C@@H](O)CO
Reaction #367110
L-arabinose hydrazone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_05
CO[C@H]1OC[C@H](O)[C@H](O)[C@H]1O
Reaction #454137
powder
收率 201.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_10
OC[C@@H](O)[C@H](O)[C@@H](O)CO
Reaction #470399
xylitol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
O=C[C@H](O)[C@H](O)[C@@H](O)[C@@H](O)CO
Reaction #524442
L-mannose
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1977_06
CO[C@H]1OC[C@H](O)[C@H](O)[C@H]1O
Reaction #565957
powder
收率 201.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_11
O=C[C@@H](O)[C@H](O)[C@H](O)CO
Reaction #712347
arabinose
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_04
CO[C@H]1OC[C@H](O)[C@H](O)[C@H]1O
Reaction #1354987
powder
收率 201.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_04
O=C[C@H](O)[C@@H](O)[C@H](O)CO
Reaction #1442506
D-xylose
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_07
O=C[C@H](O)[C@@H](O)[C@H](O)CO
Reaction #1444122
D-xylose
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_07
CO[C@H]1OC[C@H](O)[C@H](O)[C@H]1O
Reaction #1455902
powder
收率 201.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_06
O=C[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO
Reaction #1543041
glucose
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_12
CCCOC(=O)[C@H](O)[C@@H](O)[C@@H](O)CO
Reaction #1728551
1-propoxy-L-arabinose
收率 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_02
CC1(O)CCOC(=O)C1
Reaction #1779715
mevalonolactone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_04
COC(C)CN(C(=O)NCCCl)C1OC[C@H](O)[C@H](O)[C@H]1O
Reaction #1820389
1-(2-chloroethyl)-3-(2-methoxy-n-propyl)-3-(L-arabinopyranosyl)urea
收率 45.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_12
COCC(C)N(C(=O)NCCCl)C1OC[C@H](O)[C@H](O)[C@H]1O
Reaction #1820391
1-(2-chloroethyl)-3-(1-methyl-2-methoxy-ethyl)-3-(L-arabinopyranosyl)urea
收率 47.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_12
O=C(NCCCl)N(CC1CC1)C1OC[C@H](O)[C@H](O)[C@H]1O
Reaction #1820422
1-(2-chloroethyl)-3-cyclopropylmethyl-3-(L-arabinopyranosyl) urea
收率 38.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_12
O=C(NCCCl)N(Cc1ccccc1)C1OC[C@H](O)[C@H](O)[C@H]1O
Reaction #1820424
1-(2-chloroethyl)-3-benzyl-3-(L-arabinopyranosyl)urea
收率 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_12
COc1ccc(CN(C(=O)NCCCl)C2OC[C@H](O)[C@H](O)[C@H]2O)cc1
Reaction #1820426
1-(2-chloroethyl)-3-(p-methoxybenzyl)-3-(L-arabinopyranosyl)urea
收率 74.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_12
C=CCN(C(=O)NCCCl)C1OC[C@H](O)[C@H](O)[C@H]1O
Reaction #1820428
1-(2-chloroethyl)-3-(2-propenyl)-3-(L-arabinopyranosyl)urea
收率 62.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_12
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