3-methylene-cyclobutane carboxylic acid

C=C1CC(N)(C(=O)OCc2ccccc2)C1
Reaction #6044
desired compound
المردود 68.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
C=C1CC(NC(=O)OC(C)(C)C)C1
Reaction #66334
N-Boc-3-methylene-cyclobutanamine
المردود 34.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
C=C1CC(NC(=O)OC(C)(C)C)C1
Reaction #66401
N-Boc-3-methylene-cyclobutanamine
المردود 34.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
C=C1CC(NC(=O)OC(C)(C)C)C1
Reaction #155402
N-Boc-3-methylene-cyclobutanamine
المردود 34.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
C=C1CC(C(=O)NCc2nccnc2Cl)C1
Reaction #273013
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
C=C1CC(NC(=O)OC(C)(C)C)C1
Reaction #328969
N-Boc-3-methylene-cyclobutanamine
المردود 34.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
C=C1CC(C(=O)NC(c2ccc3ccc(-c4ccccc4)nc3c2)c2nccnc2Cl)C1
Reaction #331333
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
C=C1CC(C(=O)NCc2nccnc2Cl)C1
Reaction #331420
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
C=C1CC(C(=O)NCc2nccnc2Cl)C1
Reaction #331421
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
C=C1CC(NC(=O)OC(C)(C)C)C1
Reaction #331675
N-Boc-3-methylene-cyclobutanamine
المردود 34.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
C=C1CC(NC(=O)OC(C)(C)C)C1
Reaction #470761
N-Boc-3-methylene-cyclobutanamine
المردود 34.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
C=C1CC(C(=O)NC(c2ccc3ccc(-c4ccccc4)nc3c2)c2nccnc2Cl)C1
Reaction #473411
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
C=C1CC(C(=O)NCc2nccnc2Cl)C1
Reaction #473491
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
C=C1CC(C(=O)NCc2nccnc2Cl)C1
Reaction #473492
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
C=C1CC(NC(=O)OC(C)(C)C)C1
Reaction #473984
N-Boc-3-methylene-cyclobutanamine
المردود 34.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
C=C1CC(NC(=O)OC(C)(C)C)C1
Reaction #477035
N-Boc-3-methylene-cyclobutanamine
المردود 34.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
C=C1CC(C(=O)NC(c2ccc3ccc(-c4ccccc4)nc3c2)c2nccnc2Cl)C1
Reaction #509846
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
C=C1CC(C(=O)NCc2nccnc2Cl)C1
Reaction #509930
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
C=C1CC(C(=O)NCc2nccnc2Cl)C1
Reaction #509931
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
C=C1CC(NC(=O)OC(C)(C)C)C1
Reaction #533957
N-Boc-3-methylene-cyclobutanamine
المردود 34.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
الصفحة 1التالي